Electrophotographic photoconductor and aromatic polycarbonate resin for use therein

ABSTRACT

An electrophotographic photoconductor has an electroconductive support, and a photoconductive layer which is formed thereon and contains as an effective component an aromatic polycarbonate resin having a structural unit of formula (1), two structural units of formula (1) and (2), or a repeat unit of formula (3): ##STR1## wherein R 1  and R z  Ar 1  to Ar 6 , X, Y, s and n are as specified in the specification. The above-mentioned aromatic polycarbonate resin is provided with charge transporting properties.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates to an electrophoto-graphic photoconductorcomprising an electroconductive support, and a photoconductive layerformed thereon, comprising an aromatic polycarbonate resin. In addition,the present invention also relates to the above-mentioned aromaticpolycarbonate resin with charge transporting properties.

2. Discussion of Background

Recently organic photoconductors (OPC) are used in many copying machinesand printers. These organic photoconductors have a layered structurecomprising a charge generation layer (CGL) and a charge transport layer(CTL) which are successively overlaid on an electroconductive support.The charge transport layer (CTL) is a film-shaped layer comprising abinder resin and a low-molecular-weight charge transport material (CTM)dissolved therein. The addition of such a low-molecular-weight chargetransport material (CTM) to the binder resin lowers the intrinsicmechanical strength of the binder resin, so that the CTL film is fragileand has a low tensile strength. Such lowering of the mechanical strengthof the CTL causes the wearing of the photoconductor or forms scratchesand cracks on the surface of the photoconductor.

Although some vinyl polymers such as polyvinyl anthracene, polyvinylpyrene and poly-N-vinylcarbazole have been studied ashigh-molecular-weight photoconductive materials for forming a chargetransporting complex for use in the conventional organic photoconductor,such polymers are not satisfactory from the viewpoint ofphotosensitivity.

In addition, high-molecular-weight materials having charge transportingproperties have been also studied to eliminate the shortcomings of theabove-mentioned layered photoconductor. For instance, there are proposedan acrylic resin having a triphenylamine structure as reported by M.Stolka et al., in "J. Polym. Sci., vol 21, 969 (1983)"; a vinyl polymerhaving a hydrazone structure as described in "Japan Hard Copy '89 p 67";and polycarbonate resins having a triarylamine structure as disclosed inU.S. Pat. Nos. 4,801,517, 4,806,443, 4,806,444, 4,937,165, 4,959,288,5,030,532, 5,034,296, and 5,080,989, and Japanese Laid-Open PatentApplications Nos. 64-9964, 3-221522, 2-304456, 4-11627, 4-175337,4-18371, 4-31404, and 4-133065. However, any materials have not yet beenput to practical use.

According to the report of "Physical Review B46 6705 (1992)" by M. A.Abkowitz et al., it is confirmed that the drift mobility of ahigh-molecular weight charge transport material is lower than that of alow-molecular weight material by one figure. This report is based on thecomparison between the photoconductor comprising a low-molecular weighttetraarylbenzidine derivative dispersed in the photoconductive layer andthe one comprising a high-molecular polycarbonate having atetraarylbenzidine structure in its molecule. The reason for this hasnot been clarified, but it is suggested that the photoconductoremploying the high-molecular weight charge transport material producespoor results in terms of the photosensitivity and the residual potentialalthough the mechanical strength of the photoconductor is improved.

Conventionally known representative aromatic polycarbonate resins areobtained by allowing 2,2-bis (4-hydroxyphenyl) propane (hereinafterreferred to as bisphenol A) to react with phosgene or diphenylcarbonate.Such polycarbonate resins made from bisphenol A are used in many fieldsbecause of their excellent characteristics, such as high transparency,high heat resistance, high dimensional accuracy, and high mechanicalstrength.

For example, this kind of polycarbonate resin is intensively studied asa binder resin for use in an organic photoconductor in the field ofelectrophoto-graphy. A variety of aromatic polycarbonate resins havebeen proposed as the binder resins for use in the charge transport layerof the layered photoconductor.

As previously mentioned, however, the mechanical strength of theaforementioned aromatic polycarbonate resin is decreased by the additionof the low-molecular-weight charge transport material in the chargetransport layer of the layered electrophotographic photoconductor.

The electrophotographic process is one of the image formation processes,through which the surface of the photoconductor is charged uniformly inthe dark to a predetermined polarity, for instance, by corona charge.The uniformly charged photoconductor is exposed to a light image toselectively dissipate the electric charge of the light-exposed area, sothat a latent electrostatic image is formed on the photoconductor. Thethus formed latent electrostatic image is developed to a visible imageby a developer comprising a coloring agent such as a dye or pigment, anda binder agent such as a polymeric material,.

Fundamental characteristics required for the photoconductor used in suchan electrophotographic process are: (1) chargeability to an appropriatepotential in the dark, (2) minimum dissipation of electric charge in thedark, and (3) rapid dissipation of electric charge when exposed tolight.

However, the conventional photoconductive materials are not alwayssatisfactory in light of the above-mentioned fundamental characteristicsfor the photoconductor and the mechanical durability.

SUMMARY OF THE INVENTION

It is therefore a first object of the present invention to provide anelectrophotographic photoconductor free from the conventionalshortcomings, which can show high photosensitivity and high durability.

A second object of the present invention is to provide an aromaticpolycarbonate resin that is remarkably useful as a high-molecular-weightcharge transport material for use in an organic electrophotographicphotoconductor.

The above-mentioned first object of the present invention can beachieved by an electrophotographic photoconductor comprising anelectroconductive support, and a photoconductive layer formed thereoncomprising as an effective component an aromatic polycarbonate resincomprising a structural unit of formula (1): ##STR2## wherein R¹ and R²,which may be the same or different, are each a hydrogen atom, an alkylgroup which may have a substituent, or an aryl group which may have asubstituent; Ar¹, Ar², Ar³, Ar⁴, Ar⁶ and Ar⁷, which may be the same ordifferent, are each an arylene group which may have a substituent; Ar⁵and Ar⁶, which may be the same or different, are each an aryl groupwhich may have a substituent; and s is an integer of 0 or 1, and whens=1, X is --O--, --S--, --SO--, --SO₂ --, --CO--, a straight-chain,branched or cyclic alkylene group having 1 to 12 carbon atoms, or anarylene group which may have a substituent.

In the above-mentioned photoconductor, the structural unit of formula(1) may be represented by the following formula (4): ##STR3## whereinR¹, R², Ar⁵, Ar⁸ and X are the same as those previously defined informula (1).

Further, the structural unit of formula (4) may be represented byformula (6): ##STR4## wherein R¹, R², Ar⁵, Ar⁸ and X are the same asthose previously defined in formula (1).

To be more specific, the structural unit of formula (6) may berepresented by formula (B): ##STR5## wherein R¹, R² and X are the sameas those previously defined in formula (1); and R¹⁸ and R¹⁹, which maybe the same or different, are each a hydrogen atom, an alkyl group whichmay have a substituent, or an aryl group which may have a substituent.

The first object of the present invention can also be achieved by anelectrophotographic photoconductor comprising an electroconductivesupport, and a photoconductive layer formed thereon comprising as aneffective component an aromatic polycarbonate resin having theaforementioned structural unit of formula (1) and a structural unit ofthe following formula (2), with the composition ratio of the structuralunit of formula (1) to the structural unit of formula (2) satisfying arelationship of 0<k/(k+j)≦1, wherein k is the moiety ratio of thestructural unit of formula (1), and j is the moiety ratio of thestructural unit of formula (2): ##STR6## wherein Y is a bivalentaliphatic group, a bivalent cyclic aliphatic group, a bivalent aromaticgroup, a bivalent group obtained by bonding the above-mentioned bivalentgroups, or ##STR7## in which R³, R⁴, R⁵ and R⁶ are each independently analkyl group which may have a substituent, an aryl group which may have asubstituent, or a halogen atom; a and b are each independently aninteger of 0 to 4; c and d are each independently an integer of 0 to 3;and m is an integer of 0 or 1, and when m=1, Z is a straight-chainalkylene group having 2 to 12 carbon atoms, --O--, --S--, --SO--, --SO₂--, --CO--, ##STR8## in which Z¹ and Z² are each a bivalent aliphaticgroup which may have a substituent or an arylene group which may have asubstituent; and R⁷, R⁸, R⁹, R¹⁰, R¹¹, R¹² and R¹³ are eachindependently a hydrogen atom, a halogen atom, an alkyl group having 1to 5 carbon atoms which may have a substituent, an alkoxyl group having1 to 5 carbon atoms which may have a substituent, or an aryl group whichmay have a substituent, and R⁷ and R⁸ may form a carbocyclic ring orheterocyclic ring having 6 to 12 carbon atoms in combination, or mayform a carbocyclic ring or heterocyclic ring in combination with R³ andR⁴ ; p and q are each an integer of 0 or 1, when p and q represent 1,R¹⁴ and R¹⁵ are each an alkylene group having 1 to 4 carbon atoms; R¹⁶and R¹⁷ are each independently an alkyl group having 1 to 5 carbon atomswhich may have a substituent, or an aryl group which may have asubstituent; e is an integer of 0 to 4; f is an integer of 0 to 20; andg is an integer of 0 to 2000.

Furthermore the above-mentioned first object of the present inventioncan be achieved by an electrophotographic photoconductor comprising anelectroconductive support, and a photoconductive layer formed thereoncomprising as an effective component an aromatic polycarbonate resinhaving a repeat unit of formula (3): ##STR9## wherein R¹, R², Ar¹, Ar²,Ar³, Ar⁴, Ar⁵, Ar⁶, Ar⁷, Ar⁸, X and Y are the same as those previouslydefined in formulas (1) and (2): and n is an integer of 2 to 5000.

In the above-mentioned photoconductor, the repeat unit of formula (3)may be represented by the following formula (5): ##STR10## wherein R¹,R², Ar⁵, Ar⁸, X, Y and n are the same as those previously defined informula (3).

Further, the repeat unit of formula (5) may be represented by thefollowing formula (7): ##STR11## wherein R¹, R², Ar⁵, Ar⁶, X, Y and nare the same as those previously defined in formula (5).

To be more specific, the repeat unit of formula (7) may be representedby the following formula (9): ##STR12## wherein R¹, R², R₁₈, R¹⁹, X, Yand n are the same as those previously defined in formulas (8) and (2).

The second object of the present invention can be achieved by anaromatic polycarbonate resin comprising a structural unit of formula(1): ##STR13## wherein R¹ and R², which may be the same or different,are each a hydrogen atom, an alkyl group which may have a substituent,or an aryl group which may have a substituent; Ar¹, Ar², Ar³, Ar⁴, Ar⁶and Ar⁷ which may be the same or different, are each an arylene groupwhich may have a substituent; Ar⁵ and Ar⁸, which may be the same ordifferent, are each an aryl group which may have a substituent; and s isan integer of 0 or 1, and when s=1, X is --O--, --S--, --SO--, --SO₂ --,--CO--, a straight-chain, branched or cyclic alkylene group having 1 to12 carbon atoms, or an arylene group which may have a substituent.

In the above-mentioned polycarbonate resin, the structural unit offormula (1) may be represented by the above-mentioned formula (4),preferably formula (6), and further preferably formula (8).

The second object of the present invention can also be achieved by anaromatic polycarbonate resin comprising the aforementioned structuralunits of formulas (1) and (2), with the composition ratio of thestructural unit of formula (1) to the structural unit of formula (2)satisfying a relationship of 0<k/(k+j)≦1, wherein k is the moiety ratioof the structural unit of formula (1), and j is the moiety ratio of thestructural unit of formula (2).

Furthermore, the above-mentioned second object of the present inventioncan also be achieved by an aromatic polycarbonate resin comprising arepeat unit of formula (3): ##STR14## wherein R¹, R², Ar¹, Ar², Ar³,Ar⁴, Ar⁵, Ar⁶, Ar⁷, Ar⁸, X and Y are the same as those previouslydefined in formulas (1) and (2); and n is an integer of 2 to 5000.

In the above-mentioned aromatic polycarbonate resin, the repeat unit offormula (3) may be represented by the aforementioned formula (5),preferably formula (7), and more preferably formula (9).

BRIEF DESCRIPTION OF THE DRAWINGS

A more complete appreciation of the invention and many of the attendantadvantages thereof will be readily obtained as the same becomes betterunderstood by reference to the following detailed description whenconsidered in connection with the accompanying drawings, wherein:

FIG. 1 is a schematic cross-sectional view of a first example of anelectrophotographic photoconductor according to the present invention.

FIG. 2 is a schematic cross-sectional view of a second example of anelectrophotographic photoconductor according to the present invention.

FIG. 3 is a schematic cross-sectional view of a third example of anelectrophotographic photoconductor according to the present invention.

FIG. 4 is a schematic cross-sectional view of a fourth example of anelectrophotographic photoconductor according to the present invention.

FIG. 5 is a schematic cross-sectional view of a fifth example of anelectrophotographic photoconductor according to the present invention.

FIG. 6 is a schematic cross-sectional view of a sixth example of anelectrophotographic photoconductor according to the present invention.

FIGS. 7 to 9 are IR spectra of aldehyde compounds respectivelysynthesized in Preparation Examples 1-1 to 1-3, taken by use of a KBrtablet.

FIGS. 10 to 13 are IR spectra of aninostilbene compounds respectivelysynthesized in Preparation Examples 2-1 to 2-4, taken by use of a KBrtablet.

FIGS. 14 to 16 are IR spectra of diol compounds (hydroxystilbenecompounds) respectively synthesized in Preparation Examples 3-1 to 3- 3,taken by use of a KBr tablet.

FIGS. 17 to 24 are IR spectra of aromatic polycarbonate resins accordingto the present invention, respectively synthesized in Examples 1-1 to1-8, taken by use of a cast film.

DESCRIPTION OF THE PREFERRED EMBODIMENTS

The electrophotographic photoconductor according to the presentinvention comprises a photoconductive layer comprising:

(i) an aromatic polycarbonate resin comprising at least a structuralunit with the charge transporting properties, represented by formula(1), (4), (6) or (8),

(ii) an aromatic polycarbonate resin consisting of a structural unitwith the charge transporting properties, represented by formula (1),(4), (6) or (8),

(iii) an aromatic polycarbonate copolymer resin comprising a structuralunit with the charge transporting properties, represented by formula(1), (4), (6) or (8), and a structural unit of formula (2) for impartingother properties than the charge transporting properties to the obtainedresin, and

(iv) an aromatic polycarbonate alternating copolymer resin comprising arepeat unit with the charge transporting properties, represented byformula (3), (5), (7) or (9).

Those aromatic polycarbonate resins, which are novel compounds, havecharge transporting properties and high mechanical strength, so that theelectrical, optical and mechanical characteristics required for thecharge transport layer of the photoconductor are satisfactory when thepolycarbonate resins are used therein.

As previously mentioned, the aromatic polycarbonate resin of the presentinvention comprises the structural unit of formula (1): ##STR15##wherein R¹ and R², which may be the same or different, are each ahydrogen atom, an alkyl group which may have a substituent, or an arylgroup which may have a substituent; Ar¹, Ar², Ar³, Ar⁴, Ar⁶ and Ar⁷,which may be the same or different, are each an arylene group which mayhave a substituent; Ar⁵ and Ar⁸, which may be the same or different, areeach an aryl group which may have a substituent; and s is an integer of0 or 1, and when s=1, X is --O--, --S--, --SO--, --SO₂, --CO--, astraight-chain, branched or cyclic alkylene group having 1 to 12 carbonatoms, or an arylene group which may have a substituent.

It is preferable that the structural unit of formula (1) be representedby the following formula (4): ##STR16## wherein R¹, R², Ar⁵, Ar⁶ and Xare the same as those previously defined in formula (1).

Further, the structural unit of formula (4) may be represented byformula (6): ##STR17## wherein R¹, R², Ar⁵, Ar⁸ and X are the same asthose previously defined in formula (1).

To be more specific, the structural unit of formula (6) may berepresented by formula (8): ##STR18## wherein R¹, R² and X are the sameas those previously defined in formula (1); and R¹⁸ and R¹⁹, which maybe the same or different, are each a hydrogen atom, an alkyl group whichmay have a substituent, or an aryl group which may have a substituent.

In addition, the polycarbonate resin of the present invention comprisesthe repeat unit of formula (3) ##STR19## wherein R¹, R², Ar¹, Ar², Ar³,Ar⁴, Ar⁵, Ar⁶, Ar⁷, Ar⁸, X and Y are the same as those previouslydefined in formulas (1) and (2); and n is an integer of 2 to 5000.

It is preferable that the repeat unit of formula (3) be represented bythe following formula (5): ##STR20## wherein R¹, R², Ar⁵, Ar⁸, X, Y andn are the same as previously defined in formula (3).

Further, the repeat unit of formula (5) may be represented by thefollowing formula (7): ##STR21## wherein R¹, R², Ar⁵, Ar⁶, X, Y and nare the same as those previously defined in formula (5).

To be more specific, the repeat unit of formula (7) may be representedby the following formula (9): ##STR22## wherein R¹, R², R¹⁸, R¹⁹, X, Yand n are the same as those previously defined.

Those aromatic polycarbonate resins according to the present inventioncan be obtained by the method of synthesizing a conventionalpolycarbonate resin, that is, polymerization of a bisphenol and acarbonic acid derivative.

To be more specific, the aromatic polycarbonate resin of the presentinvention can be produced by the ester interchange between a diolcompound having the charge transporting properties, represented by thefollowing formula (10), (11), (12) or (13) and a bisarylcarbonatecompound, or by the polymerization of the above-mentioned diol compoundwith a halogenated carbonyl compound such as phosgene in accordance withsolution polymerization or interfacial polymerization, or by thepolymerization of the above-mentioned diol compound with abischloroformate compound derived from a diol compound in accordancewith solution polymerization or interfacial polymerization. ##STR23##wherein R¹ and R², Ar¹ to Ar⁶, R¹⁸, and R¹⁹, X are the same as thosepreviously defined in formulas (1) and (8).

In addition to the phosgene, trichloromethyl chloroformate that is adimer of phosgene, and bis (trichloromethyl) carbonate that is a trimerof phosgene are usable as the halogenated carbonyl compounds in theabove-mentioned polymerization. Further, halogenated carbonyl compoundsderived from other halogen atoms than chlorine, for example, carbonylbromide, carbonyl iodide and carbonyl fluoride are also employed.

Those conventional synthesis methods are described in the reference,such as "Handbook of Polycarbonate Resin" (issued by The Nikkan KogyoShimbun Ltd.).

When a diol of the following formula (14) is employed in combinationwith the diol of formula (10), (11), (12) or (13) with the chargetransporting properties in the course of the polymerization, there canbe produced a copolymer polycarbonate resin with improved mechanicalcharacteristics. In this case, a plurality of kinds of diol compoundsrepresented by formula (14) may be employed.

    OH--Y--OH                                                  (14)

wherein Y is the same as that previously defined in formula (2).

In such a synthesis method, the amount ratio of the diol represented byformula (10), (11), (12) or (13) which is provided with the chargetransporting properties to the diol of formula (14) can be selectedwithin a wide range in light of the desired characteristics of theobtained aromatic polycarbonate resin. Further, a variety of copolymers,such as a random copolymer, an alternating copolymer, a block copolymer,a random alternating copolymer, or a random block copolymer can beobtained according to the polymerization procedure.

For instance, a random copolymer comprising the structural unit offormula (1), (4), (6) or (8) and the structural unit of formula (2) canbe obtained when the diol of formula (10), (11), (12) or (13) with thecharge transporting properties and the diol of formula (14) areuniformly mixed prior to the condensation reaction with the phosgene. Arandom block copolymer can be obtained by adding several diols in thecourse of the polymerization reaction. Further, an alternating copolymercomprising a repeat unit of formula (3), (5), (7) or (9) can be producedby carrying out the condensation reaction of a bischloroformate compoundderived from the diol of formula (14) with the diol having the chargetransporting properties, represented by formula (10), (11), (12) or(13). In such a case, the above-mentioned mentioned alternatingcopolymer comprising a repeat unit of formula (3), (5), (7) or (9) canbe similarly produced by carrying out the condensation reaction of abischloroformate compound derived from the diol of formula (10), (11),(12) or (13) with the diol of formula (14). Further, a randomalternating copolymer can be produced by employing a plurality ofbischloroformate compounds and diol compounds in the course of theaforementioned condensation reaction between the bischloroformatecompound and the diol.

The interfacial polymerization is carried out at the interface betweentwo phases of an alkaline aqueous solution of a diol and an organicsolvent which is substantially incompatible with water and capable ofdissolving a polycarbonate therein in the presence of the carbonic acidderivative and a catalyst. In this case, a polycarbonate resin with anarrow molecular-weight weight distribution can be speedily obtained byemulsifying the reactive medium through high-speed stirring operation oraddition of an emulsifying material.

As a base for preparing the aforementioned alkaline aqueous solution,there can be employed an alkali metal and an alkaline earth metal.Specific examples of the base include hydroxides such as sodiumhydroxide, potassium hydroxide and calcium hydroxide; and carbonatessuch as sodium carbonate, potassium carbonate, calcium carbonate andsodium hydrogencarbonate. Those bases may be used alone or incombination. Of those bases, sodium hydroxide and potassium hydroxideare preferable. In addition, distilled water or ion exchange water arepreferably employed for the preparation of the above-mentioned alkalineaqueous solution.

Examples of the organic solvent used in the above-mentioned interfacialpolymerization are aliphatic halogenated hydrocarbon solvents such as1,2-dichloroethane, 1,2-dichloroethylene, dichloroethylene,trichloroethane, tetrachloroethane and dichloropropane; aromatichalogenated hydrocarbon solvents such as chlorobenzene anddichlorobenzene; and mixed solvents thereof. Further, aromatichydrocarbon solvents such as toluene, xylene and ethylbenzene, andaliphatic hydrocarbon solvents such as hexane and cyclohexane may beadded to the above-mentioned solvents. Of those organic solvents, thealiphatic halogenated hydrocarbon solvents and aromatic halogenatedhydrocarbon solvents, in particular, dichloromethane and chlorobenzeneare preferable in the present invention.

Examples of the catalyst used in the preparation of the polycarbonateresin are a tertiary amine, a quaternary ammonium salt, a tertiaryphosphine, a quaternary phosphonium salt, a nitrogen-containingheterocyclic compound and salts thereof, an iminoether and saltsthereof, and a compound having amide group.

Specific examples of such a catalyst used in the interfacialpolymerization include trimethylamine, triethylamine, tri-n-propylamine,tri-n-hexylamine, N,N,N',N'-tetramethyl-1, 4-tetramethylene-diamine,4-pyrrolidinopyridine, N,N'-dimethylpiperazine, N-ethylpiperidine,benzyltrimethylammonium chloride, benzyltriethylammonium chloride,tetramethylammonium chloride, tetraethylammonium bromide,phenyltriethylammonium chloride, triethylphosphine, triphenylphosphine,diphenylbutylphosphine tetra(hydroxymethyl)phosphonium chloride,benzyltriethylphosphonium chloride, benzyltriphenylphosphonium chloride,4-methylpyridine, 1-methylimidazole, 1,2-dimethylimidazole,3-methylpyridazine, 4,6-dimethylpyrimidine,1-cyclohexyl-3,5-dimethylpyrazole, and 2,3,5,6-tetramethylpyrazine.

Those catalysts may be used alone or in combination. Of theabove-mentioned catalysts, the tertiary amine, in particular, a tertiaryamine having 3 to 30 carbon atoms, such as triethylamine is preferablyemployed in the present invention. Before and/or after the carbonic acidderivatives such as phosgene and bischloroformate are placed in thereaction system, any of the above-mentioned catalysts may be addedthereto.

To control the molecular weight of the obtained polycarbonate resin, itis desirable to employ a terminator as a molecular weight modifier forany of the above-mentioned polymerization reactions. Consequently, asubstituent derived from the terminator may be bonded to the end of themolecule of the obtained polycarbonate resin.

As the terminator for use in the present invention, a monovalentaromatic hydroxy compound and haloformate derivatives thereof, and amonovalent carboxylic acid and halide derivatives thereof can be usedalone or in combination.

Specific examples of the monovalent aromatic hydroxy compound arephenols such as phenol, p-cresol, o-ethylphenol, p-ethylphenol,p-isopropylphenol, p-tert-butylphenol, p-cumylphenol,p-cyclohexylphenol, p-octylphenol, p-nonylphenol, 2,4-xylenol,p-methoxyphenol, p-hexyloxyphenol, p-decyloxyphenol, o-chlorophenol,m-chlorophenol, p-chlorophenol, p-bromophenol, pentabromophenol,pentachlorophenol, p-phenylphenol, p-isopropenylphenol,2,4-di(1'-methyl-1'-phenyleyhyl) phenol, β-naphthol, α-naphthol,p-(2',4',4'-trimethylchromanyl)phenol, and 2-(4'-methoxyphenyl)-2-(4"-hydroxyphenyl)propane. In addition, alkali metal salts andalkaline earth metal salts of the above phenols can also be employed.

Specific examples of the monovalent carboxylic acid are aliphatic acidssuch as acetic acid, propionic acid, butyric acid, valeric acid, caproicacid, heptanic acid, caprylic acid, 2,2-dimethylpropionic acid,3-methylbutyric acid, 3,3-dimethylbutyric acid, 4-methylvaleric acid,3,3-dimethylvaleric acid, 4-methylcaproic acid, 3,5-dimethylcaproic acidand phenoxyacetic acid; and benzoic acids such as p-methylbenzoic acid,p-tert-butylbenzoic acid, p-butoxybenzoic acid, p-octyloxybenzoic acid,p-phenylbentoic acid, p-benzylbenzoic acid and p-chlorobenzoic acid. Inaddition, alkali metal salts and alkaline earth metal salts of theabove-mentioned aliphatic acids and benzoic acids can also be employedas the terminators.

Of those terminators, the monovalent aromatic hydroxy compound, inparticular, phenol, p-tert-butylphenol, or p-cumylphenol is preferable.

It is preferable that the aromatic polycarbonate resin for use in thephotoconductor of the present invention have a number-average molecularweight of 1,000 to 500,000, more preferably in the range of 10,000 to200,000 when expressed by the styrene-reduced value.

Furthermore, a branching agent may be added in a small amount during thepolymerization in order to improve the mechanical properties of theobtained polycarbonate resin. Any compounds having three or morereactive groups, which may be the same or different, selected from thegroup consisting of an aromatic hydroxyl group, a haloformate group, acarboxylic acid group, a carboxylic acid halide group, and an activehalogen atom can be used as the branching agents for use in the presentinvention.

Specific examples of the branching agent for use in the presentinvention are as follows:

phloroglucinol,

4,6-dimethyl-2,4,6-tris (4'-hydroxyphenyl)-2-heptene,

4,6-dimethyl-2,4,6-tris(4'-hydroxyphenyl)heptane,

1,3,5-tris(4'-hydroxyphenyl)benzene,

1,1,1-tris(4'-hydroxyphenyl)ethane,

1,1,2-tris(4'-hydroxyphenyl)propane,

α,α, α'-tris(4'-hydroxyphenyl)-1-ethyl-4-isopropylbenzene,

2,4-bis[α-methyl-α-(4'-hydroxyphenyl) ethyl]phenol,

2-(4'-hydroxyphenyl)-2-(2", 4"-dihydroxyphenyl)-propane,

tris(4-hydroxyphenyl)phosphine,

1,1,4,4-tetrakis(4'-hydroxyphenyl)cyclohexane,

2,2-bis[4',4'-bis(4"-hydroxyphenyl)cyclohexyl]-propane,

α,α,α',α'-tetrakis(4'-hydroxyphenyl)-1,4-diethylbenzene,

2,2,5,5-tetrakis(4'-hydroxyphenyl)hexane,

1,1,2,3-tetrakis(4'-hydroxyphenyl)propane,

1,4-bis(4', 4"-dihydroxytriphenylmethyl)benzene,

3,3',5,5'-tetrahydroxydiphenyl ether,

3,5-dihydroxybenzoic acid,

3,5-bis(chlorocarbonyloxy)benzoic acid,

4-hydroxyisophthalic acid,

4-chlorocarbonyloxyisophthalic acid,

5-hydroxyphthalic acid,

5-chlorocarbonyloxyphthalic acid,

trimesic trichloride, and

cyanuric chloride.

Those branching agents may be used alone or in combination.

To prevent the oxidation of the dial in the alkaline aqueous solution,an antioxidant such as hydrosulfite may be used in the interfacialpolymerization reaction.

The interfacial polymerization reaction is generally carried out attemperature in the range of 0 to 40° C., and terminated in severalminutes to 5 hours. It is desirable to maintain the reaction system topH 10 or more.

In the case of the solution polymerization, the diol is dissolved in aproper solvent to prepare a solution of the diol, and a deacidifyingagent is added thereto. Then, the bischloroformate compound, or thephosgene (or dimer and trimer thereof) is added to the above preparedmixture. In this case, tertiary amine compounds such as trimethylamine,triethylamine and tripropylamine, and pyridine can be used as thedeacidifying agents. Examples of the solvent for use in theabove-mentioned solution polymerization are halogenated hydrocarbonsolvents such as dichloromethane, dichloroethane, trichloroethane,tetrachloroethane, trichloroethylene, and chloroform; cyclic ethers suchas tetrahydrofuran and dioxane; and pyridine. In addition, the samemolecular weight modifier and branching agent as those employed in theinterfacial polymerization can be used. The reaction temperature of thesolution polymerization is generally in the range of 0 to 40° C. In thiscase, the polymerization is generally terminated in several minutes to 5hours.

In the case where the polycarbonate resin is synthesized by the esterinterchange method, the diol and the bisarylcarbonate are mixed in thepresence of an inert gas, and the reaction is carried out at atemperature in the range of 120 to 350° C. under reduced pressure. Thepressure in the reaction system is stepwise reduced to 1 mmHg or less inorder to distill away the phenols generated during the reaction from thereaction system. The reaction is commonly terminated in about one to 4hours. When necessary, the molecular weight modifier and the antioxidantmay be added to the reaction system. As the bisarylcarbonate compound,diphenyl carbonate, di-p-tolyl carbonate, phenyl-p-totyl carbonate,di-p-chlorophenyl carbonate and dinaphthyl carbonate can be employed.

The polycarbonate resin thus synthesized is purified by removing thecatalyst and the antioxidant used in the polymerization; unreacted dioland terminator; and impurities such as an inorganic salt generatedduring the polymerization, and then subjected to the preparation of thephotoconductive layer of the electrophotographic photoconductoraccording to the present invention. The previously mentioned "Handbookof Polycarbonate Resin" (issued by Nikkan Kogyo Shimbun Ltd.) can bereferred to for such a procedure for purifying the polycarbonate resin.

To the aromatic polycarbonate resin produced by the previously mentionedmethods, various additives such as an antioxidant, a light stabilizer, athermal stabilizer, a lubricant and a plasticizer can be added whennecessary.

The structural unit of formula (1) for use in the polycarbonate resinaccording to the present invention will now be explained in detail.

In the formula (1), the alkyl group represented by R¹ and R² is astraight-chain or branched alkyl group having 1 to 5 carbon atoms. Theabove alkyl group may have a substituent such as a halogen atom, or aphenyl group which may have a substituent of a straight-chain orbranched alkyl group having 1 to 5 carbon atoms.

Specific examples of the above alkyl group represented by R¹ and R²include methyl group, ethyl group, n-propyl group, isopropyl group,tert-butyl group, sec-butyl group, n-butyl group, isobutyl group,trifluoromethyl group, benzyl group, 4-chlorobenzyl group, and4-methylbenzyl group.

As the aryl group represented by R¹, R², Ar⁵ and Ar⁶, there can beemployed phenyl group, naphthyl group, and biphenylyl group. The arylgroup may have as a substituent the above-mentioned substituted orunsubstituted alkyl group.

Specific examples of the aryl group represented by R¹, R², Ar⁵ and Ar⁸include phenyl group, 4-methylphenyl group and 4'-methyl-4-biphenylylgroup.

As the substituted or unsubstituted arylene group represented by Ar¹,Ar², Ar³, Ar⁴, Ar⁶, Ar⁷ and X, the bivalent groups derived from thesubstituted or unsubstituted aryl group defined in the description ofR¹, R², Ar⁵ and Ar⁸.

Specific examples of the alkylene group represented by X includemethylene group, ethylene group, 1,3-propylene group, 2,2-propylenegroup and 1,1-cyclohexylene group.

In other formulas than the formula (1), the same examples as defined inthe description of formula (1) can be employed so long as the symbolsuch as R¹, R² or Ar¹ for use in the formula is identical.

Specific examples of the diol compound represented by formula (10),which is a raw material for the preparation of the polycarbonate resinaccording to the present invention, are shown in TABLE 1.

    TABLE 1       -      ##STR24##     1     Diol       Comp       No. Ar.sup.3 Ar.sup.4 Ar.sup.5 Ar.sup.6 Ar.sup.7 Ar.sup.8       1      ##STR25##     2      ##STR26##     2      ##STR27##     3      ##STR28##     2      ##STR29##     2      ##STR30##     3     2      ##STR31##     2      ##STR32##     2      ##STR33##     3      ##STR34##     2      ##STR35##     2      ##STR36##     3     3      ##STR37##     2      ##STR38##     2      ##STR39##     3      ##STR40##     2      ##STR41##     2      ##STR42##     3     4      ##STR43##     2      ##STR44##     2      ##STR45##     3      ##STR46##     2      ##STR47##     2      ##STR48##     3     5      ##STR49##     2      ##STR50##     2      ##STR51##     3      ##STR52##     2      ##STR53##     2      ##STR54##     3     6      ##STR55##     2      ##STR56##     2      ##STR57##     3      ##STR58##     2      ##STR59##     2      ##STR60##     3     7      ##STR61##     2      ##STR62##     2      ##STR63##     3      ##STR64##     2      ##STR65##     2      ##STR66##     3     8      ##STR67##     2      ##STR68##     2      ##STR69##     3      ##STR70##     2      ##STR71##     2      ##STR72##     3     9      ##STR73##     2      ##STR74##     2      ##STR75##     3      ##STR76##     2      ##STR77##     2      ##STR78##     3     10      ##STR79##     2      ##STR80##     2      ##STR81##     3      ##STR82##     2      ##STR83##     2      ##STR84##     3     11      ##STR85##     2      ##STR86##     2      ##STR87##     3      ##STR88##     2      ##STR89##     2      ##STR90##     3     12      ##STR91##     2      ##STR92##     2      ##STR93##     3      ##STR94##     2      ##STR95##     2      ##STR96##     3     13      ##STR97##     2      ##STR98##     2      ##STR99##     3      ##STR100##     2      ##STR101##     2      ##STR102##     3     14      ##STR103##     2      ##STR104##     2      ##STR105##     3      ##STR106##     2      ##STR107##     2      ##STR108##     3     15      ##STR109##     2      ##STR110##     2      ##STR111##     3      ##STR112##     2      ##STR113##     2      ##STR114##     3     16      ##STR115##     2      ##STR116##     2      ##STR117##     8      ##STR118##     2      ##STR119##     2      ##STR120##     8     17      ##STR121##     2      ##STR122##     2      ##STR123##     9      ##STR124##     2      ##STR125##     2      ##STR126##     9     18      ##STR127##     2      ##STR128##     2      ##STR129##     8      ##STR130##     2      ##STR131##     2      ##STR132##     8     19      ##STR133##     2      ##STR134##     2      ##STR135##     8      ##STR136##     2      ##STR137##     2      ##STR138##     8     20      ##STR139##     2      ##STR140##     2      ##STR141##     8      ##STR142##     2      ##STR143##     2      ##STR144##     8     21      ##STR145##     2      ##STR146##     2      ##STR147##     8      ##STR148##     2      ##STR149##     2      ##STR150##     8     22      ##STR151##     2      ##STR152##     2      ##STR153##     8      ##STR154##     2      ##STR155##     2      ##STR156##     8     23      ##STR157##     2      ##STR158##     2      ##STR159##     8      ##STR160##     2      ##STR161##     2      ##STR162##     8     24      ##STR163##     2      ##STR164##      ##STR165##     3      ##STR166##      ##STR167##     2      ##STR168##     3     25      ##STR169##     2      ##STR170##     2      ##STR171##     3      ##STR172##     2      ##STR173##     2      ##STR174##     3     26      ##STR175##     2      ##STR176##     2      ##STR177##     3      ##STR178##     2      ##STR179##     2      ##STR180##     3     27      ##STR181##     2      ##STR182##     2      ##STR183##     3      ##STR184##     2      ##STR185##     2      ##STR186##     3     28      ##STR187##     2      ##STR188##     2      ##STR189##     3      ##STR190##     2      ##STR191##     2      ##STR192##     3     29      ##STR193##     2      ##STR194##     2      ##STR195##     3      ##STR196##     2      ##STR197##     2      ##STR198##     3     30      ##STR199##     2      ##STR200##     2      ##STR201##     3      ##STR202##     2      ##STR203##     2      ##STR204##     3     31      ##STR205##     2      ##STR206##     2      ##STR207##     3      ##STR208##     2      ##STR209##     2      ##STR210##     3     32      ##STR211##     2      ##STR212##     2      ##STR213##     3      ##STR214##     2      ##STR215##     2      ##STR216##     3     33      ##STR217##     2      ##STR218##     2      ##STR219##     3      ##STR220##     2      ##STR221##     2      ##STR222##     3     34      ##STR223##     2      ##STR224##     2      ##STR225##     3      ##STR226##     2      ##STR227##     2      ##STR228##     3     35      ##STR229##     2      ##STR230##     2      ##STR231##     3      ##STR232##     2      ##STR233##     2      ##STR234##     3     36      ##STR235##     2      ##STR236##     2      ##STR237##     3      ##STR238##     2      ##STR239##     2      ##STR240##     3     37      ##STR241##     2      ##STR242##     2      ##STR243##     3      ##STR244##     2      ##STR245##     2      ##STR246##     3     38      ##STR247##     2      ##STR248##     2      ##STR249##     3      ##STR250##     2      ##STR251##     2      ##STR252##     3     39      ##STR253##     2      ##STR254##     2      ##STR255##     3      ##STR256##     2      ##STR257##     2      ##STR258##     3     40      ##STR259##     2      ##STR260##     2      ##STR261##     3      ##STR262##     2      ##STR263##     2      ##STR264##     3     41      ##STR265##     2      ##STR266##     2      ##STR267##     3      ##STR268##     2      ##STR269##     2      ##STR270##     3     42      ##STR271##     2      ##STR272##     2      ##STR273##     3      ##STR274##     2      ##STR275##     2      ##STR276##     3     43      ##STR277##     2      ##STR278##     2      ##STR279##     3      ##STR280##     2      ##STR281##     2      ##STR282##     3     44      ##STR283##     2      ##STR284##     2      ##STR285##     8      ##STR286##     2      ##STR287##     2      ##STR288##     8     45      ##STR289##     2      ##STR290##     2      ##STR291##     9      ##STR292##     2      ##STR293##     2      ##STR294##     9     46      ##STR295##     2      ##STR296##     2      ##STR297##     8      ##STR298##     2      ##STR299##     2      ##STR300##     8     47      ##STR301##     2      ##STR302##     2      ##STR303##     8      ##STR304##     2      ##STR305##     2      ##STR306##     8     48      ##STR307##     2      ##STR308##     2      ##STR309##     8      ##STR310##     2      ##STR311##     2      ##STR312##     8     49      ##STR313##     2      ##STR314##     2      ##STR315##     8      ##STR316##     2      ##STR317##     2      ##STR318##     8     50      ##STR319##     2      ##STR320##     2      ##STR321##     8      ##STR322##     2      ##STR323##     2      ##STR324##     8     51      ##STR325##     2      ##STR326##     2      ##STR327##     8      ##STR328##     2      ##STR329##     2      ##STR330##     8     52      ##STR331##     2      ##STR332##      ##STR333##     3      ##STR334##      ##STR335##     2      ##STR336##     3     53      ##STR337##     2      ##STR338##     2      ##STR339##     3      ##STR340##     2      ##STR341##     2      ##STR342##     3     54      ##STR343##     2      ##STR344##     2      ##STR345##     3      ##STR346##     2      ##STR347##     2      ##STR348##     3     55      ##STR349##     2      ##STR350##     2      ##STR351##     3      ##STR352##     2      ##STR353##     2      ##STR354##     3     56      ##STR355##     2      ##STR356##     2      ##STR357##     3      ##STR358##     2      ##STR359##     2      ##STR360##     3     57      ##STR361##     2      ##STR362##     2      ##STR363##     3      ##STR364##     2      ##STR365##     2      ##STR366##     3     58      ##STR367##     2      ##STR368##     2      ##STR369##     3      ##STR370##     2      ##STR371##     2      ##STR372##     3     59      ##STR373##     2      ##STR374##     2      ##STR375##     3      ##STR376##     2      ##STR377##     2      ##STR378##     3     60      ##STR379##     2      ##STR380##     2      ##STR381##     3      ##STR382##     2      ##STR383##     2      ##STR384##     3     61      ##STR385##     2      ##STR386##     2      ##STR387##     3      ##STR388##     2      ##STR389##     2      ##STR390##     3     62      ##STR391##     2      ##STR392##     2      ##STR393##     3      ##STR394##     2      ##STR395##     2      ##STR396##     3     63      ##STR397##     2      ##STR398##     2      ##STR399##     3      ##STR400##     2      ##STR401##     2      ##STR402##     3     64      ##STR403##     2      ##STR404##     2      ##STR405##     8      ##STR406##     2      ##STR407##     2      ##STR408##     8     65      ##STR409##     2      ##STR410##     2      ##STR411##     9      ##STR412##     2      ##STR413##     2      ##STR414##     9     66      ##STR415##     2      ##STR416##     2      ##STR417##     3      ##STR418##     2      ##STR419##     2      ##STR420##     3     67      ##STR421##     2      ##STR422##     2      ##STR423##     3      ##STR424##     2      ##STR425##     2      ##STR426##     3     68      ##STR427##     2      ##STR428##     2      ##STR429##     3      ##STR430##     2      ##STR431##     2      ##STR432##     3     69      ##STR433##     2      ##STR434##     2      ##STR435##     3      ##STR436##     2      ##STR437##     2      ##STR438##     3     70      ##STR439##     2      ##STR440##     2      ##STR441##     3      ##STR442##     2      ##STR443##     2      ##STR444##     3     71      ##STR445##     2      ##STR446##     2      ##STR447##     3      ##STR448##     2      ##STR449##     2      ##STR450##     3     72      ##STR451##     2      ##STR452##     2      ##STR453##     3      ##STR454##     2      ##STR455##     2      ##STR456##     3     73      ##STR457##     2      ##STR458##     2      ##STR459##     8      ##STR460##     2      ##STR461##     2      ##STR462##     8     74      ##STR463##     2      ##STR464##     2      ##STR465##     9      ##STR466##     2      ##STR467##     2      ##STR468##     9       Diol       Comp       No. R.sup.1 R.sup.2 A B X       1 H H      ##STR469##     4      ##STR470##     4  --CH.sub.2 CH.sub.2      --                           2 H H      ##STR471##     5      ##STR472##     4  --CH.sub.2 CH.sub.2      --                           3 H H      ##STR473##     5      ##STR474##     5  --CH.sub.2 CH.sub.2      --                           4 H H      ##STR475##     4      ##STR476##     4  --CH.sub.2      --                  5 H H      ##STR477##     5      ##STR478##     5  --CH.sub.2      --                  6 H H      ##STR479##     4      ##STR480##     4      ##STR481##     6     7 H H      ##STR482##     5      ##STR483##     5      ##STR484##     6     8 H H      ##STR485##     4      ##STR486##     4  --CH.sub.2 CH.sub.2 CH.sub.2      --                                    9 H H      ##STR487##     5      ##STR488##     5  --CH.sub.2 CH.sub.2 CH.sub.2      --                                    10 H H      ##STR489##     4      ##STR490##     4      ##STR491##     7     11 H H      ##STR492##     5      ##STR493##     5      ##STR494##     7     12 H H      ##STR495##     4      ##STR496##     4  --O--     13 H H      ##STR497##     5      ##STR498##     5  --O--     14 H H      ##STR499##     4      ##STR500##     4  --S--     15 H H      ##STR501##     5      ##STR502##     5  --S--     16 H H      ##STR503##     4      ##STR504##     4  --CH.sub.2 CH.sub.2      --                           17 H H      ##STR505##     4      ##STR506##     4  --CH.sub.2 CH.sub.2      --                           18 H H      ##STR507##     4      ##STR508##     4  --CH.sub.2      --                  19 H H      ##STR509##     4      ##STR510##     4      ##STR511##     6     20 H H      ##STR512##     4      ##STR513##     4  --CH.sub.2 CH.sub.2 CH.sub.2      --                                    21 H H      ##STR514##     4      ##STR515##     4      ##STR516##     7     22 H H      ##STR517##     4      ##STR518##     4  --O--     23 H H      ##STR519##     4      ##STR520##     4  --S--     24 H H      ##STR521##     4      ##STR522##     4  --CH.sub.2 CH.sub.2      --                           25 H H      ##STR523##     4      ##STR524##     4      ##STR525##     1     26 H H      ##STR526##     5      ##STR527##     5      ##STR528##     1     27 H H      ##STR529##     4      ##STR530##     4      ##STR531##     2     28 H H      ##STR532##     5      ##STR533##     5      ##STR534##     2     29      ##STR535##     3      ##STR536##     3      ##STR537##     4      ##STR538##     4  --CH.sub.2 CH.sub.2      --                           30      ##STR539##     3      ##STR540##     3      ##STR541##     5      ##STR542##     4  --CH.sub.2 CH.sub.2      --                           31      ##STR543##     3      ##STR544##     3      ##STR545##     5      ##STR546##     5  --CH.sub.2 CH.sub.2      --                           32      ##STR547##     3      ##STR548##     3      ##STR549##     4      ##STR550##     4  --CH.sub.2      --                  33      ##STR551##     3      ##STR552##     3      ##STR553##     5      ##STR554##     5  --CH.sub.2      --                  34      ##STR555##     3      ##STR556##     3      ##STR557##     4      ##STR558##     4      ##STR559##     6     35      ##STR560##     3      ##STR561##     3      ##STR562##     5      ##STR563##     5      ##STR564##     6     36      ##STR565##     3      ##STR566##     3      ##STR567##     4      ##STR568##     4  --CH.sub.2 CH.sub.2 CH.sub.2      --                                    37      ##STR569##     3      ##STR570##     3      ##STR571##     5      ##STR572##     5  --CH.sub.2 CH.sub.2 CH.sub.2      --                                    38      ##STR573##     3      ##STR574##     3      ##STR575##     4      ##STR576##     4      ##STR577##     7     39      ##STR578##     3      ##STR579##     3      ##STR580##     5      ##STR581##     5      ##STR582##     7     40      ##STR583##     3      ##STR584##     3      ##STR585##     4      ##STR586##     4  --O--     41      ##STR587##     3      ##STR588##     3      ##STR589##     5      ##STR590##     5  --O--     42      ##STR591##     3      ##STR592##     3      ##STR593##     4      ##STR594##     4  --S--     43      ##STR595##     3      ##STR596##     3      ##STR597##     5      ##STR598##     5  --S--     44      ##STR599##     3      ##STR600##     3      ##STR601##     4      ##STR602##     4  --CH.sub.2 CH.sub.2      --                           45      ##STR603##     3      ##STR604##     3      ##STR605##     4      ##STR606##     4  --CH.sub.2 CH.sub.2      --                           46      ##STR607##     3      ##STR608##     3      ##STR609##     4      ##STR610##     4  --CH.sub.2 CH.sub.2      --                           47      ##STR611##     3      ##STR612##     3      ##STR613##     4      ##STR614##     4      ##STR615##     6     48      ##STR616##     3      ##STR617##     3      ##STR618##     4      ##STR619##     4  --CH.sub.2 CH.sub.2 CH.sub.2      --                                    49      ##STR620##     3      ##STR621##     3      ##STR622##     4      ##STR623##     4      ##STR624##     7     50      ##STR625##     3      ##STR626##     3      ##STR627##     4      ##STR628##     4  --O--     51      ##STR629##     3      ##STR630##     3      ##STR631##     4      ##STR632##     4  --S--     52      ##STR633##     3      ##STR634##     3      ##STR635##     4      ##STR636##     4  --CH.sub.2 CH.sub.2      --                           53      ##STR637##     3      ##STR638##     3      ##STR639##     4      ##STR640##     4      ##STR641##     1     54      ##STR642##     3      ##STR643##     3      ##STR644##     5      ##STR645##     5      ##STR646##     1     55      ##STR647##     3      ##STR648##     3      ##STR649##     4      ##STR650##     4      ##STR651##     2     56      ##STR652##     3      ##STR653##     3      ##STR654##     5      ##STR655##     5      ##STR656##     2     57 CH.sub.3 CH.sub.3      ##STR657##     4      ##STR658##     4  --CH.sub.2 CH.sub.2      --                           58 CH.sub.3 CH.sub.3      ##STR659##     4      ##STR660##     4   CH.sub.2      --                 59 CH.sub.3 CH.sub.3      ##STR661##     4      ##STR662##     4      ##STR663##     6     60 CH.sub.3 CH.sub.3      ##STR664##     4      ##STR665##     4  --CH.sub.2 CH.sub.2 CH.sub.2      --                                    61 CH.sub.3 CH.sub.3      ##STR666##     4      ##STR667##     4      ##STR668##     7     62 CH.sub.3 CH.sub.3      ##STR669##     4      ##STR670##     4  --O--     63 CH.sub.3 CH.sub.3      ##STR671##     4      ##STR672##     4  --S--     64 CH.sub.3 CH.sub.3      ##STR673##     4      ##STR674##     4  --CH.sub.2 CH.sub.2      --                           65 CH.sub.3 CH.sub.3      ##STR675##     4      ##STR676##     4  --CH.sub.2 CH.sub.2      --                           66      ##STR677##     8      ##STR678##     8      ##STR679##     4      ##STR680##     4  --CH.sub.2 CH.sub.2      --                           67      ##STR681##     8      ##STR682##     8      ##STR683##     4      ##STR684##     4  --CH.sub.2      --                  68      ##STR685##     8      ##STR686##     8      ##STR687##     4      ##STR688##     4      ##STR689##     6     69      ##STR690##     8      ##STR691##     8      ##STR692##     4      ##STR693##     4  --CH.sub.2 CH.sub.2 CH.sub.2      --                                    70      ##STR694##     8      ##STR695##     8      ##STR696##     4      ##STR697##     4      ##STR698##     7     71      ##STR699##     8      ##STR700##     8      ##STR701##     4      ##STR702##     4  --O--     72      ##STR703##     8      ##STR704##     8      ##STR705##     4      ##STR706##     4  --S--     73      ##STR707##     8      ##STR708##     8      ##STR709##     4      ##STR710##     4  --CH.sub.2 CH.sub.2      --                           74      ##STR711##     8      ##STR712##     8      ##STR713##     4      ##STR714##     4  --CH.sub.2 CH.sub.2      --                           75      ##STR715##     8      ##STR716##     8      ##STR717##     4      ##STR718##     4  --CH.sub.2 CH.sub.2      --                           76      ##STR719##     8      ##STR720##     8      ##STR721##     4      ##STR722##     4  --CH.sub.2 CH.sub.2      --

The diols represented by the formulas (10), (11), (12) and (13), whichare intermediates for preparation of the aromatic polycarbonate resinsaccording to the present invention, will now be explained in detail.

The above-mentioned diols (10), (11), (12) and (13) are hydroxystilbenecompounds, which are novel compounds.

Those hydroxystilbene compounds are obtained from aminostilbenecompounds by dealkylation or deacylation. The aminostilbene compounds offormulas (15), ((17), (17) and (18), serving as the intermediates forthe hydroxystilbene compounds of formulas (10), (11), (12) and (13), areas follows: ##STR723## wherein R¹ and R², which may be the same ordifferent, are each a hydrogen atom, an alkyl group which may have asubstituent, or an aryl group which may have a substituent; R²⁰ and R²¹,which may be the same or different, are each an alkyl group which mayhave a substituent or an acyl group which may have a substituent; Ar¹,Ar², Ar³, Ar⁴, Ar⁶ and Ar⁷, which may be the same or different, are eachan arylene group which may have a substituent; Ar⁵ and Ar⁸, which may bethe same or different, are each an aryl group which may have asubstituent; and s is an integer of 0 or 1 and when s=1, X is --O--,--S--, --SO--, --SO₂ --, --CO--, a straight-chain, branched or cyclicalkylene group hating 1 to 12 carbon atoms, or an arylene group whichmay have a substituent. ##STR724## wherein R¹ and R², R²⁰ and R²¹, Ar⁵and Ar⁸, and X are the same as those previously defined in formula (15).##STR725## wherein R¹, R², R²⁰, R²¹, Ar⁵, Ar⁸, and X are the same asthose previously defined in formula (15). ##STR726## wherein R¹, R², R¹⁸and R¹⁹, which may be the same or different, are each a hydrogen atom,an alkyl group which may have a substituent, or an aryl group which mayhave a substituent; R²⁰ and R²¹, which may be the same or different, areeach an alkyl group which may have a substituent or an acyl group whichmay have a substituent; and s is an integer of 0 or 1, and when s=1, Xis --O--, --S--, --SO--, --S₂ --, --CO--, a straight-chain, branched orcyclic alkylene group having 1 to 12 carbon atoms, or an arylene groupwhich may have a substituent.

To carry out the dealkylation of the aminostilbene compounds, thecleavage reaction in the aminostilbene compound is performed using anacidic reagent or a basic reagent.

Specific examples of the acidic reagent used in the cleavage reactionare hydrogen bromide, hydrogen iodide, trifluoroacetic acid,hydrochloride of pyridine, concentrated hydrochloric acid, magnesiumiodide ethylate, aluminum chloride, aluminum bromide, boron tribromide,boron trichloride, and boron triiodide.

Specific examples of the basic reagent are potassium hydroxide, lithiumdiphenyl phosphide, and sodium thiolate.

For the above-mentioned cleavage reaction, a solvent such asdichloromethane, tetrahydrofuran (THF), N,N-dimethylformamide (DME),pyridine or butanol can be employed. The reaction temperature, whichvaries depending on the activity of the employed reagent, is generallyin the range of room temperature to 200° C.

As previously mentioned, the hydroxystilbene compound can be obtained bythe deacylation of the aminostilbene compound. In this case, deacylationmay be carried out using an acidic reagent such as hydrochloric acid orsulfuric acid, and a basic reagent such as sodium hydroxide or potassiumhydroxide. As the solvent, there can be employed methanol, ethanol,isopropanol, butanol, 2-methoxyethanol, 1,2-dimethoxyethane, bis(2-methoxyethyl) ether, dioxane, tetrahydrofuran, benzene, toluene,xylene, dimethyl sulfoxide, N,N-dimethylformatamide,N-methylpyrrolidone, and 1,3-dimethyl-2-imidazolydinone.

The above-mentioned aminostilbene compound can be obtained by allowingan aldehyde compound represented by the following formula (19) to reactwith a phosphorus-containing compound represented by the followingformulas (20a) and (20b) in the presence of a basic catalyst at atemperature in the range of room temperature to about 100° C.:##STR727## wherein Ar³, Ar⁴, Ar⁶ and Ar⁷, which may be the same ordifferent, are each an arylene group which may have a substituent; Ar⁵and Ar⁸, which may be the same or different, are each an aryl groupwhich may have a substituent; and s is an integer of 0 or 1, and whens=1, X is --O--, --S--, --SO----SO₂ --, --CO--, a straight-chain,branched or cyclic alkylene group having 1 to 12 carbon atoms, or anarylene group which may have a substituent. ##STR728## wherein R¹ and R²are each a hydrogen atom, an alkyl group which may have a substituent,or an aryl group which may have a substituent; R²⁰ and R²¹ are each analkyl group which may have a substituent or an acyl group which may havea substituent; Ar¹ and Ar² are each an arylene group which may have asubstituent; and A represents (i) a phosphonium salt of formula --P⁺(R²²)₃ B⁻⁻, in which R²² is phenyl group or a lower alkyl group, and Bis a halogen atom; or (ii) a dialkyl phosphorous acid group of formula--PO(OR²³)₂, in which R²³ is a lower alkyl group.

In the above-mentioned reaction for preparation of the aminostilbenecompound, phenyl lithium, sodium hydroxide, potassium hydroxide, sodiumamide, sodium hydride, and alcoholates such as sodium methylate andpotassium-t-butoxide can be used as the basic catalysts.

Examples of the reaction solvent used in the above-mentioned reactionare methanol, ethanol, isopropanol, butanol, 2-methoxyethanol,1,2-dimethoxyethane, bis(2-methoxyethyl)ether, dioxane, tetrahydrofuran,benzene, toluene, xylene, dimethyl sulfoxide, N,N-dimethylformamide,N-methylpyrrolidone and 1,3-dimethyl-2-imidazolidinone. Of thesesolvents, a polar solvent such as N,N-dimethylformamide or dimethylsulfoxide is preferably employed.

The reaction temperature in the above-mentioned reaction may bedetermined within a wide range depending on (i) the stability of theemployed solvent with respect to the employed basic catalyst, (ii) thereactivity of the condensed components, that is, the above-mentionedcompounds (19), (20a) and (20b), and (iii) the reactivity of theemployed basic catalyst as a condensation agent in the solvent. Forinstance, when a polar solvent is employed, the reaction temperature isin the range of room temperature to 100° C., preferably in the range ofroom temperature to 80° C. The reaction temperature may be furtherincreased when it is desired to curtail the reaction time, or theactivity of a condensation agent to be employed is low. Specificexamples of the aminostilbene compound thus obtained are shown in TABLE2.

    TABLE 2       -      ##STR729##     1     Amino-       stil-       bene       Comp       No. Ar.sup.3 Ar.sup.4 Ar.sup.5 Ar.sup.6 Ar.sup.7 Ar.sup.8       1      ##STR730##     2      ##STR731##     2      ##STR732##     3      ##STR733##     2      ##STR734##     2      ##STR735##     3     2      ##STR736##     2      ##STR737##     2      ##STR738##     3      ##STR739##     2      ##STR740##     2      ##STR741##     3     3      ##STR742##     2      ##STR743##     2      ##STR744##     3      ##STR745##     2      ##STR746##     2      ##STR747##     3     4      ##STR748##     2      ##STR749##     2      ##STR750##     3      ##STR751##     2      ##STR752##     2      ##STR753##     3     5      ##STR754##     2      ##STR755##     2      ##STR756##     3      ##STR757##     2      ##STR758##     2      ##STR759##     3     6      ##STR760##     2      ##STR761##     2      ##STR762##     3      ##STR763##     2      ##STR764##     2      ##STR765##     3     7      ##STR766##     2      ##STR767##     2      ##STR768##     3      ##STR769##     2      ##STR770##     2      ##STR771##     3     8      ##STR772##     2      ##STR773##     2      ##STR774##     3      ##STR775##     2      ##STR776##     2      ##STR777##     3     9      ##STR778##     2      ##STR779##     2      ##STR780##     3      ##STR781##     2      ##STR782##     2      ##STR783##     3     10      ##STR784##     2      ##STR785##     2      ##STR786##     3      ##STR787##     2      ##STR788##     2      ##STR789##     3     11      ##STR790##     2      ##STR791##     2      ##STR792##     3      ##STR793##     2      ##STR794##     2      ##STR795##     3     12      ##STR796##     2      ##STR797##     2      ##STR798##     3      ##STR799##     2      ##STR800##     2      ##STR801##     3     13      ##STR802##     2      ##STR803##     2      ##STR804##     3      ##STR805##     2      ##STR806##     2      ##STR807##     3     14      ##STR808##     2      ##STR809##     2      ##STR810##     3      ##STR811##     2      ##STR812##     2      ##STR813##     3     15      ##STR814##     2      ##STR815##     2      ##STR816##     3      ##STR817##     2      ##STR818##     2      ##STR819##     3     16      ##STR820##     2      ##STR821##     2      ##STR822##     8      ##STR823##     2      ##STR824##     2      ##STR825##     8     17      ##STR826##     2      ##STR827##     2      ##STR828##     9      ##STR829##     2      ##STR830##     2      ##STR831##     9     18      ##STR832##     2      ##STR833##     2      ##STR834##     8      ##STR835##     2      ##STR836##     2      ##STR837##     8     19      ##STR838##     2      ##STR839##     2      ##STR840##     8      ##STR841##     2      ##STR842##     2      ##STR843##     8     20      ##STR844##     2      ##STR845##     2      ##STR846##     8      ##STR847##     2      ##STR848##     2      ##STR849##     8     21      ##STR850##     2      ##STR851##     2      ##STR852##     8      ##STR853##     2      ##STR854##     2      ##STR855##     8     22      ##STR856##     2      ##STR857##     2      ##STR858##     8      ##STR859##     2      ##STR860##     2      ##STR861##     8     23      ##STR862##     2      ##STR863##     2      ##STR864##     8      ##STR865##     2      ##STR866##     2      ##STR867##     8     24      ##STR868##     2      ##STR869##     2      ##STR870##     3      ##STR871##     2      ##STR872##     2      ##STR873##     3     25      ##STR874##     2      ##STR875##      ##STR876##     3      ##STR877##      ##STR878##     2      ##STR879##     3     26      ##STR880##     2      ##STR881##     2      ##STR882##     3      ##STR883##     2      ##STR884##     2      ##STR885##     3     27      ##STR886##     2      ##STR887##     2      ##STR888##     3      ##STR889##     2      ##STR890##     2      ##STR891##     3     28      ##STR892##     2      ##STR893##     2      ##STR894##     3      ##STR895##     2      ##STR896##     2      ##STR897##     3     29      ##STR898##     2      ##STR899##     2      ##STR900##     3      ##STR901##     2      ##STR902##     2      ##STR903##     3     30      ##STR904##     2      ##STR905##     2      ##STR906##     3      ##STR907##     2      ##STR908##     2      ##STR909##     3     31      ##STR910##     2      ##STR911##     2      ##STR912##     3      ##STR913##     2      ##STR914##     2      ##STR915##     3     32      ##STR916##     2      ##STR917##     2      ##STR918##     3      ##STR919##     2      ##STR920##     2      ##STR921##     3     33      ##STR922##     2      ##STR923##     2      ##STR924##     3      ##STR925##     2      ##STR926##     2      ##STR927##     3     34      ##STR928##     2      ##STR929##     2      ##STR930##     3      ##STR931##     2      ##STR932##     2      ##STR933##     3     35      ##STR934##     2      ##STR935##     2      ##STR936##     3      ##STR937##     2      ##STR938##     2      ##STR939##     3     36      ##STR940##     2      ##STR941##     2      ##STR942##     3      ##STR943##     2      ##STR944##     2      ##STR945##     3     37      ##STR946##     2      ##STR947##     2      ##STR948##     3      ##STR949##     2      ##STR950##     2      ##STR951##     3     38      ##STR952##     2      ##STR953##     2      ##STR954##     3      ##STR955##     2      ##STR956##     2      ##STR957##     3     39      ##STR958##     2      ##STR959##     2      ##STR960##     3      ##STR961##     2      ##STR962##     2      ##STR963##     3     40      ##STR964##     2      ##STR965##     2      ##STR966##     3      ##STR967##     2      ##STR968##     2      ##STR969##     3     41      ##STR970##     2      ##STR971##     2      ##STR972##     3      ##STR973##     2      ##STR974##     2      ##STR975##     3     42      ##STR976##     2      ##STR977##     2      ##STR978##     3      ##STR979##     2      ##STR980##     2      ##STR981##     3     43      ##STR982##     2      ##STR983##     2      ##STR984##     3      ##STR985##     2      ##STR986##     2      ##STR987##     3     44      ##STR988##     2      ##STR989##     2      ##STR990##     3      ##STR991##     2      ##STR992##     2      ##STR993##     3     45      ##STR994##     2      ##STR995##     2      ##STR996##     8      ##STR997##     2      ##STR998##     2      ##STR999##     8     46      ##STR1000##     2      ##STR1001##     2      ##STR1002##     9      ##STR1003##     2      ##STR1004##     2      ##STR1005##     9     47      ##STR1006##     2      ##STR1007##     2      ##STR1008##     8      ##STR1009##     2      ##STR1010##     2      ##STR1011##     8     48      ##STR1012##     2      ##STR1013##     2      ##STR1014##     8      ##STR1015##     2      ##STR1016##     2      ##STR1017##     8     49      ##STR1018##     2      ##STR1019##     2      ##STR1020##     8      ##STR1021##     2      ##STR1022##     2      ##STR1023##     8     50      ##STR1024##     2      ##STR1025##     2      ##STR1026##     8      ##STR1027##     2      ##STR1028##     2      ##STR1029##     8     51      ##STR1030##     2      ##STR1031##     2      ##STR1032##     8      ##STR1033##     2      ##STR1034##     2      ##STR1035##     8     52      ##STR1036##     2      ##STR1037##     2      ##STR1038##     8      ##STR1039##     2      ##STR1040##     2      ##STR1041##     8     53      ##STR1042##     2      ##STR1043##     2      ##STR1044##     3      ##STR1045##     2      ##STR1046##     2      ##STR1047##     3     54      ##STR1048##     2      ##STR1049##      ##STR1050##     3      ##STR1051##      ##STR1052##     2      ##STR1053##     3     55      ##STR1054##     2      ##STR1055##     2      ##STR1056##     3      ##STR1057##     2      ##STR1058##     2      ##STR1059##     3     56      ##STR1060##     2      ##STR1061##     2      ##STR1062##     3      ##STR1063##     2      ##STR1064##     2      ##STR1065##     3     57      ##STR1066##     2      ##STR1067##     2      ##STR1068##     3      ##STR1069##     2      ##STR1070##     2      ##STR1071##     3     58      ##STR1072##     2      ##STR1073##     2      ##STR1074##     3      ##STR1075##     2      ##STR1076##     2      ##STR1077##     3     59      ##STR1078##     2      ##STR1079##     2      ##STR1080##     3      ##STR1081##     2      ##STR1082##     2      ##STR1083##     3     60      ##STR1084##     2      ##STR1085##     2      ##STR1086##     3      ##STR1087##     2      ##STR1088##     2      ##STR1089##     3     61      ##STR1090##     2      ##STR1091##     2      ##STR1092##     3      ##STR1093##     2      ##STR1094##     2      ##STR1095##     3     62      ##STR1096##     2      ##STR1097##     2      ##STR1098##     3      ##STR1099##     2      ##STR1100##     2      ##STR1101##     3     63      ##STR1102##     2      ##STR1103##     2      ##STR1104##     3      ##STR1105##     2      ##STR1106##     2      ##STR1107##     3     64      ##STR1108##     2      ##STR1109##     2      ##STR1110##     3      ##STR1111##     2      ##STR1112##     2      ##STR1113##     3     65      ##STR1114##     2      ##STR1115##     2      ##STR1116##     3      ##STR1117##     2      ##STR1118##     2      ##STR1119##     3     66      ##STR1120##     2      ##STR1121##     2      ##STR1122##     8      ##STR1123##     2      ##STR1124##     2      ##STR1125##     8     67      ##STR1126##     2      ##STR1127##     2      ##STR1128##     9      ##STR1129##     2      ##STR1130##     2      ##STR1131##     9     68      ##STR1132##     2      ##STR1133##     2      ##STR1134##     3      ##STR1135##     2      ##STR1136##     2      ##STR1137##     3     69      ##STR1138##     2      ##STR1139##     2      ##STR1140##     3      ##STR1141##     2      ##STR1142##     2      ##STR1143##     3     70      ##STR1144##     2      ##STR1145##     2      ##STR1146##     3      ##STR1147##     2      ##STR1148##     2      ##STR1149##     3     71      ##STR1150##     2      ##STR1151##     2      ##STR1152##     3      ##STR1153##     2      ##STR1154##     2      ##STR1155##     3     72      ##STR1156##     2      ##STR1157##     2      ##STR1158##     3      ##STR1159##     2      ##STR1160##     2      ##STR1161##     3     73      ##STR1162##     2      ##STR1163##     2      ##STR1164##     3      ##STR1165##     2      ##STR1166##     2      ##STR1167##     3     74      ##STR1168##     2      ##STR1169##     2      ##STR1170##     3      ##STR1171##     2      ##STR1172##     2      ##STR1173##     3     75      ##STR1174##     2      ##STR1175##     2      ##STR1176##     8      ##STR1177##     2      ##STR1178##     2      ##STR1179##     8     76      ##STR1180##     2      ##STR1181##     2      ##STR1182##     9      ##STR1183##     2      ##STR1184##     2      ##STR1185##     9       Amino-       stil-       bene       Comp       No. R.sup.1 R.sup.2 A B X       1 H H      ##STR1186##     4      ##STR1187##     4  --CH.sub.2 CH.sub.2      --                           2 H H      ##STR1188##     5      ##STR1189##     4  --CH.sub.2 CH.sub.2      --                           3 H H      ##STR1190##     5      ##STR1191##     5  --CH.sub.2 CH.sub.2      --                           4 H H      ##STR1192##     4      ##STR1193##     4  --CH.sub.2      --                  5 H H      ##STR1194##     5      ##STR1195##     5  --CH.sub.2      --                  6 H H      ##STR1196##     4      ##STR1197##     4      ##STR1198##     6     7 H H      ##STR1199##     5      ##STR1200##     5      ##STR1201##     6     8 H H      ##STR1202##     4      ##STR1203##     4  --CH.sub.2 CH.sub.2 CH.sub.2      --                                    9 H H      ##STR1204##     5      ##STR1205##     5  --CH.sub.2 CH.sub.2 CH.sub.2      --                                    10 H H      ##STR1206##     4      ##STR1207##     4      ##STR1208##     7     11 H H      ##STR1209##     5      ##STR1210##     5      ##STR1211##     7     12 H H      ##STR1212##     4      ##STR1213##     4  --O--     13 H H      ##STR1214##     5      ##STR1215##     5  --O--     14 H H      ##STR1216##     4      ##STR1217##     4  --S--     15 H H      ##STR1218##     5      ##STR1219##     5  --S--     16 H H      ##STR1220##     4      ##STR1221##     4  --CH.sub.2 CH.sub.2      --                           17 H H      ##STR1222##     4      ##STR1223##     4  --CH.sub.2 CH.sub.2      --                           18 H H      ##STR1224##     4      ##STR1225##     4  --CH.sub.2 CH.sub.2      --                           19 H H      ##STR1226##     4      ##STR1227##     4      ##STR1228##     6     20 H H      ##STR1229##     4      ##STR1230##     4  --CH.sub.2 CH.sub.2 CH.sub.2      --                                    21 H H      ##STR1231##     4      ##STR1232##     4      ##STR1233##     7     22 H H      ##STR1234##     4      ##STR1235##     4  --O--     23 H H      ##STR1236##     4      ##STR1237##     4  --S--     24 H H      ##STR1238##     1      ##STR1239##     1  --CH.sub.2 CH.sub.2      --                           25 H H      ##STR1240##     4      ##STR1241##     4  --CH.sub.2 CH.sub.2      --                           26 H H      ##STR1242##     4      ##STR1243##     4      ##STR1244##     2     27 H H      ##STR1245##     5      ##STR1246##     5      ##STR1247##     2     28 H H      ##STR1248##     4      ##STR1249##     4      ##STR1250##     3     29 H H      ##STR1251##     5      ##STR1252##     5      ##STR1253##     3     30      ##STR1254##     3      ##STR1255##     3      ##STR1256##     4      ##STR1257##     4  --CH.sub.2 CH.sub.2      --                           31      ##STR1258##     3      ##STR1259##     3      ##STR1260##     5      ##STR1261##     4  --CH.sub.2 CH.sub.2      --                           32      ##STR1262##     3      ##STR1263##     3      ##STR1264##     5      ##STR1265##     5  --CH.sub.2 CH.sub.2      --                           33      ##STR1266##     3      ##STR1267##     3      ##STR1268##     4      ##STR1269##     4  --CH.sub.2      --                  34      ##STR1270##     3      ##STR1271##     3      ##STR1272##     5      ##STR1273##     5  --CH.sub.2      --                  35      ##STR1274##     3      ##STR1275##     3      ##STR1276##     4      ##STR1277##     4      ##STR1278##     6     36      ##STR1279##     3      ##STR1280##     3      ##STR1281##     5      ##STR1282##     5      ##STR1283##     6     37      ##STR1284##     3      ##STR1285##     3      ##STR1286##     4      ##STR1287##     4  --CH.sub.2 CH.sub.2 CH.sub.2      --                                    38      ##STR1288##     3      ##STR1289##     3      ##STR1290##     5      ##STR1291##     5  --CH.sub.2 CH.sub.2 CH.sub.2      --                                    39      ##STR1292##     3      ##STR1293##     3      ##STR1294##     4      ##STR1295##     4      ##STR1296##     7     40      ##STR1297##     3      ##STR1298##     3      ##STR1299##     5      ##STR1300##     5      ##STR1301##     7     41      ##STR1302##     3      ##STR1303##     3      ##STR1304##     4      ##STR1305##     4  --O--     42      ##STR1306##     3      ##STR1307##     3      ##STR1308##     5      ##STR1309##     5  --O--     43      ##STR1310##     3      ##STR1311##     3      ##STR1312##     4      ##STR1313##     4  --S--     44      ##STR1314##     3      ##STR1315##     3      ##STR1316##     5      ##STR1317##     5  --S--     45      ##STR1318##     3      ##STR1319##     3      ##STR1320##     4      ##STR1321##     4  --CH.sub.2 CH.sub.2      --                           46      ##STR1322##     3      ##STR1323##     3      ##STR1324##     4      ##STR1325##     4  --CH.sub.2 CH.sub.2      --                           47      ##STR1326##     3      ##STR1327##     3      ##STR1328##     4      ##STR1329##     4  --CH.sub.2      --                  48      ##STR1330##     3      ##STR1331##     3      ##STR1332##     4      ##STR1333##     4      ##STR1334##     6     49      ##STR1335##     3      ##STR1336##     3      ##STR1337##     4      ##STR1338##     4  --CH.sub.2 CH.sub.2 CH.sub.2      --                                    50      ##STR1339##     3      ##STR1340##     3      ##STR1341##     4      ##STR1342##     4      ##STR1343##     7     51      ##STR1344##     3      ##STR1345##     3      ##STR1346##     4      ##STR1347##     4  --O--     52      ##STR1348##     3      ##STR1349##     3      ##STR1350##     4      ##STR1351##     4  --S--     53      ##STR1352##     3      ##STR1353##     3      ##STR1354##     1      ##STR1355##     1  --CH.sub.2 CH.sub.2      --                           54      ##STR1356##     3      ##STR1357##     3      ##STR1358##     4      ##STR1359##     4  --CH.sub.2 CH.sub.2      --                           55      ##STR1360##     3      ##STR1361##     3      ##STR1362##     4      ##STR1363##     4      ##STR1364##     2     56      ##STR1365##     3      ##STR1366##     3      ##STR1367##     5      ##STR1368##     5      ##STR1369##     2     57      ##STR1370##     3      ##STR1371##     3      ##STR1372##     4      ##STR1373##     4      ##STR1374##     3     58      ##STR1375##     3      ##STR1376##     3      ##STR1377##     5      ##STR1378##     5      ##STR1379##     3     59 CH.sub.3 CH.sub.3      ##STR1380##     4      ##STR1381##     4  --CH.sub.2 CH.sub.2      --                           60 CH.sub.3 CH.sub.3      ##STR1382##     4      ##STR1383##     4  --CH.sub.2      --                  61 CH.sub.3 CH.sub.3      ##STR1384##     4      ##STR1385##     4      ##STR1386##     6     62 CH.sub.3 CH.sub.3      ##STR1387##     4      ##STR1388##     4  --CH.sub.2 CH.sub.2 CH.sub.2      --                                    63 CH.sub.3 CH.sub.3      ##STR1389##     4      ##STR1390##     4      ##STR1391##     7     64 CH.sub.3 CH.sub.3      ##STR1392##     4      ##STR1393##     4  --O--     65 CH.sub.3 CH.sub.3      ##STR1394##     4      ##STR1395##     4  --S--     66 CH.sub.3 CH.sub.3      ##STR1396##     4      ##STR1397##     4  --CH.sub.2 CH.sub.2      --                           67 CH.sub.3 CH.sub.3      ##STR1398##     4      ##STR1399##     4  --CH.sub.2 CH.sub.2      --                           68      ##STR1400##     8      ##STR1401##     8      ##STR1402##     4      ##STR1403##     4  --CH.sub.2 CH.sub.2      --                           69      ##STR1404##     8      ##STR1405##     8      ##STR1406##     4      ##STR1407##     4  --CH.sub.2      --                  70      ##STR1408##     8      ##STR1409##     8      ##STR1410##     4      ##STR1411##     4      ##STR1412##     6     71      ##STR1413##     8      ##STR1414##     8      ##STR1415##     4      ##STR1416##     4  --CH.sub.2 CH.sub.2 CH.sub.2      --                                    72      ##STR1417##     8      ##STR1418##     8      ##STR1419##     4      ##STR1420##     4      ##STR1421##     7     73      ##STR1422##     8      ##STR1423##     8      ##STR1424##     4      ##STR1425##     4  --O--     74      ##STR1426##     8      ##STR1427##     8      ##STR1428##     4      ##STR1429##     4  --S--     75      ##STR1430##     8      ##STR1431##     8      ##STR1432##     4      ##STR1433##     4  --CH.sub.2 CH.sub.2      --                           76      ##STR1434##     8      ##STR1435##     8      ##STR1436##     4      ##STR1437##     4  --CH.sub.2 CH.sub.2      --

The previously mentioned hydroxystilbene compounds and aminostilbenecompounds for use in the present invention, which are remarkablyeffective as photoconductive materials in the electrophotographicphotoconductor, are optically or chemically sensitized with a sensitizersuch as a dye or Lewis acid. In particular, the hydroxystilbenecompounds and aminostilbene compounds effectively function as chargetransport materials in a function-separating type electrophotographicphotoconductor where an organic or inorganic pigment serves as a chargegeneration material.

In this case, there can be employed as the sensitizer triarylmethanedyes such as Methyl Violet and Crystal Violet; xanthene dyes such asRose Bengale, Erythrosin and Rhodamine B; thiazine dyes such asMethylene Blue; and 2,4,7-trinitro-9-fluorenone and2,4-dinitro-9-fluorenone.

In addition, specific examples of the charge generation material used inthe above-mentioned function-separating photoconductor include organicpigments, for example, an azo pigment such as C.I. Pigment Blue 25 (C.I.21180), C.I. Pigment Red 41 (C.I. 21200) and C.I. Basic Red 3 (C.I.45210), a phthalocyanine pigment such as C.I. Pigment Blue 16 (C.I.74100), an indigo pigment such as C.I. Vat Brown 5 (C.I. 73410) and C.I.Vat Dye (C.I. 73030), and a perylene pigment such as Algol Scarlet B andIndanthrene Scarlet R (made by Bayer Co., Ltd.); and inorganic pigmentssuch as selenium, selenium-tellurium, tellurium, cadmium sulfide, anda-silicon (amorphous silicon).

Furthermore, a variety of materials such as a polycarbonate resin,polyester resin, polyurethane resin and epoxy resin can be obtained byderiving from the hydroxyl group of the above-mentioned hydroxystilbenecompound. In other words, the hydroxystilbene compound for use in thepresent invention is considered to be useful as an intermediate for thepreparation of those materials, in particular, the aromaticpolycarbonate resin of the present invention.

The previously mentioned aldehyde compound represented by formula (19),which is a raw material for the aminostilbene compound of formula (15)will now be explained in detail. ##STR1438## wherein Ar³, Ar⁴, Ar⁶ andAr⁷, which may be the same or different, are each an arylene group whichmay have a substituent; Ar⁵ and A⁸, which may be the same or different,are each an aryl group which may have a substituent; and s is an integerof 0 or 1, and when s=1, X is --O--, --S--, --SO--, --SO₂ --, --CO--, astraight-chain, branched or cyclic alkylene group having 1 to 12 carbonatoms, or an arylene group which may have a substituent.

To be more specific, the following aldehyde compounds of formulas (21)and (22) are usable for the preparation of the aminostilbene compoundsin the present invention. ##STR1439## wherein Ar⁵ and Ar⁸, which may bethe same or different, are each an aryl group which may have asubstituent; R³¹, R³², R³³, R³⁴, R³⁵ and R³⁶, which may be the same ordifferent, are each a hydrogen atom, an alkyl group which may have asubstituent, or an alkoxyl group which may have a substituent; and s isan integer of 0 or 1, and when s=1, X is --O--, --S--, --SO--, --SO₂ --,--CO--, a straight-chain, branched or cyclic alkylene group having 1 to12 carbon atoms, or an arylene group which may have a substituent.

In the above formulas (21) and (22), specific examples of the alkylgroup represented by R³¹, R³², R³³, R³⁴, R³⁵ and R³⁶ are lower alkylgroups such as methyl group, ethyl group, propyl group, and butyl group;and specific examples of the alkoxyl group represented by R³¹, R³², R³³,R³⁴, R³⁵ and R³⁶ are lower alkoxyl groups such as methoxy group, ethoxygroup, and propoxy group. Further, the above-mentioned alkyl group mayhave a substituent such as phenyl group, a halogen atom, an alkoxylgroup or an aryloxy group.

The aldehyde compound of formula (19) for use in the present inventionis obtained by formylation of a diamine compound, to be more specific,by allowing a diamine compound of the following formula (23) to reactwith a Vilsmeier reagent to produce an inmonium salt intermediate, andthe obtained immonium salt is subjected to hydrolysis. ##STR1440##wherein Ar³ to Ar⁸, and X are the same as those previously defined informula (19).

The aforementioned Vilsmeier reagent for use in the present inventioncan be prepared by the conventional method, that is, by allowing anamide compound such as N,N-dimethylformamide (DMF) orN-methylformanilide (MFA) to react with an acid halide such asphosphoryl chloride, phosphoryl bromide, oxalyl chloride, phosgene,thionyl chloride, triphenylphosphine-Br, or hexachlorotriphosphazatrienein an amount equivalent to the above amide compound.

The Vilsmeier reagent may be added in a stoichiometric amount to thediamine compound of formula (23), preferably in an amount of 2 mole ormore to one mole of the diamine compound.

For producing the aldehyde compound of formula (19) for use in thepresent invention, the Vilsmeier reagent which has been previouslyprepared is allowed to react with the diamine compound of formula (23)in a proper solvent. Alternatively, the above-mentioned acid halide isadded dropwise to a solution in which the diamine compound of formula(23) and the above-mentioned amide compound are dissolved, therebycarrying out the reaction as generating the Vilsmeier reagent.

In the above reaction for the preparation of the aldehyde compound, aninert aromatic hydrocarbon such as benzene, chloroform, dichloroethane,and o-dichlorobenzene are usable as the reaction solvents. Further, theabove-mentioned amide compounds may be used as the reaction solvents asthey are.

The reaction temperature is generally in the range of 0 to 150° C.,preferably in the range of 20 to 80° C.

The immonium salt thus generated by the above-mentioned reaction betweenthe diamine compound and the Vilsmeier reagent is subjected tohydrolysis in water or an alkaline aqueous solution, so that thealdehyde compound represented by the formula (19) is derived. In thiscase, an aqueous solution of sodium hydroxide, potassium hydroxide,sodium acetate, or potassium acetate can be used as the alkaline aqueoussolution.

Likewise, the previously mentioned aldehyde compounds of formulas (21)and (22) can be obtained by formylation of the following diaminecompounds of formulas (24) and (25), respectively. ##STR1441## whereinAr⁵, Ar⁸, R³¹, R³², R³³, R³⁴, R³⁵, R³⁶, and X are the same as thosepreviously defined.

Specific examples of the thus prepared aldehyde compound of formula (22)are shown in TABLE 3.

                                      TABLE 3                                     __________________________________________________________________________    3  STR1442##                                                                    -                                                                           Alde-                                                                                                      hyde                                               Comp.                                                                         No. R.sup.31 R.sup.32  R.sup.35 R.sup.34 R.sup.33  R.sup.36 X               __________________________________________________________________________    1   H   H   H   H   W   H   --CH.sub.2 CH.sub.2 --                              2 H H 4-CH.sub.3 H H 4-CH.sub.3 --CH.sub.2 CH.sub.2 --                        3 H H 4-OCH.sub.3 H H 4-OCH.sub.3 --CH.sub.2 CH.sub.2 --                      4 H H 4-C.sub.2 H.sub.5 H H 4-C.sub.2 H.sub.5 --CH.sub.2 CH.sub.2 --                                     5 3-CH.sub.3 H 3-CH.sub.3 H 3-CH.sub.3                                       3-CH.sub.3 --CH.sub.2 CH.sub.2 --                   6 2-CH.sub.3 2-CH.sub.3 4-CH.sub.3 2-CH.sub.3 2-CH.sub.3 4-CH.sub.3                                     --CH.sub.2 CH.sub.2 --                              7 H H H H H H --O--                                                           8 H H 4-CH.sub.3 H H 4-CH.sub.3 --O--                                         9 H H 4-OCH.sub.3 H H 4-OCH.sub.3 --O--                                       10 H H 4-C.sub.2 H.sub.5 H H 4-C.sub.2 H.sub.5                                11 3-CH.sub.3 H 3-CH.sub.3 H 3-CH.sub.3 3-CH.sub.3 --O--                      12 2-CH.sub.3 2-CH.sub.3 4-CH.sub.3 2-CH.sub.3 2-CH.sub.3 4-CH.sub.3                                    --O--                                               13 H H H H H H --S--                                                          14 H H 4-CH.sub.3 H H 4-CH.sub.3 --S--                                        15 H H 4-OCH.sub.3 H H 4-OCH.sub.3 --S--                                      16 H H 4-C.sub.2 H.sub.5 H H 4-C.sub.2 H.sub.3 --S--                          17 3-CH.sub.3 H 3-CH.sub.3 H 3-CH.sub.3 3-CH.sub.3 --S--                      18 2-CH.sub.3 2-CH.sub.3 4-CH.sub.5 2-CH.sub.3 2-CH.sub.3 4-CH.sub.3                                    --S--                                               19 H H H H H H --SO--                                                         20 H H H H H H --SO.sub.2 --                                                  21 H H H H H H --CO--                                                         22 H H H H H H --CH.sub.2 CH.sub.2 CH.sub.2 CH.sub.2 --                     __________________________________________________________________________

According to the present invention, the polycarbonate resin for use inthe photoconductive layer of the photoconductor comprises the structuralunit of formula (1) which is provided with the charge transportingproperties. To control the mechanical characteristics of the obtainedpolycarbonate resin, a copolymer resin comprising one structural unit offormula (1) and the other structural unit for use in the conventionallyknown polycarbonate resin, for example, as described in the previouslymentioned "Handbook of Polycarbonate Resin" (issued by The Nikkan KogyoShimbun Ltd.) can be employed. The structural unit of formula (2) is oneof the conventionally known structural units for use in the conventionalpolycarbonate resin, which can be preferably employed in the presentinvention.

The structural unit of formula (2) will now be explained by referring tothe diol of formula (14) that is the starting material for thestructural unit of formula (2).

    HO--Y--OH                                                  (14)

In the case where Y in the diol of formula (14) represents a bivalentaliphatic group or bivalent cyclic aliphatic group, the representativeexamples of the obtained diol are as follows: ethylene glycol,diethylene glycol, triethylene glycol, polyethylene glycol,polytetramethylene ether glycol, 1,3-propanediol, 1,4-butanediol,1,5-pentanediol, 3-methyl-1,5-pentanediol, 1,6-hexanediol,1,5-hexanediol, 1,7-heptanediol, 1,8-octanediol, 1,9-nonanediol,1,10-decanediol, 1,11-undecanediol, 1,12-dodecanediol, neopentyl glycol,2-ethyl-1,6-hexanediol, 2-methyl-1,3-propanediol,2-ethyl-1,3-propanediol, 2,2-dimethyl-1,3-propanediol,1,3-cyclohexanediol, 1,4-cyclohexanediol, cyclohexane-1,4-dimethanol,2,2-bis(4-hydroxycyclohexyl)propane, xylylenediol,1,4-bis(2-hydroxythyl)benzene, 1,4-bis(3-hydroxypropyl)benzene,1,4-bis(4-hydroxybutyl)benzene, 1,4-bis (5-hydroxypentyl)benzene, and1,4-bis (6-hydroxyhexyl)benzene.

In the case where Y in the diol of formula (14) represents a bivalentaromatic group, there can be employed any bivalent groups derived fromthe same substituted or unsubstituted aryl group as defined in thedescription of R¹, R², Ar⁵ and Ar⁸. In addition, Y represents thefollowing bivalent groups: ##STR1443## in which R³, R⁴, R⁵ and R⁶ areeach independently an alkyl group which may have a substituent, an arylgroup which may have a substituent, or a halogen atom; a and b are eachindependently an integer of 0 to 4; c and d are each independently aninteger of 0 to 3; and m is an integer of 0 or 1, and when m=1, Z is astraight-chain alkylene group having 2 to 12 carbon atoms, --O--, --S--,--SO--, --SO₂ --, --CO--, ##STR1444## in which Z¹ and Z² are each abivalent aliphatic group which may have a substituent or an arylenegroup which may have a substituent; and R⁷, R⁸, R⁹, R¹⁰, R¹¹, R¹² andR¹³ are each independently a hydrogen atom, a halogen atom, an alkylgroup having 1 to 5 carbon atoms which may have a substituent, analkoxyl group having 1 to 5 carbon atoms which may have a substituent,or an aryl group which may have a substituent, and R⁷ and R⁸ may form acarbocyclic ring or heterocyclic ring having 6 to 12 carbon atoms incombination, or may form a carbocyclic ring or heterocyclic ring incombination with R³ and R⁴ ; p and q are each an integer of 0 or 1, whenp and q represent 1, R¹⁴ and R¹⁵ are each an alkylene group having 1 to4 carbon atoms; R¹⁶ and R¹⁷ are each independently an alkyl group having1 to 5 carbon atoms which may have a substituent, or an aryl group whichmay have a substituent; e is an integer of 0 to 4; f is an integer of 0to 20; and g is an integer of 0 to 2000.

In the above-mentioned bivalent groups, the same substituted orunsubstituted alkyl group, and the same substituted or unsubstitutedaryl group as defined in the description of R¹, R², Ar⁵ and Ar⁸ in thestructural unit of formula (1) can be employed.

Examples of the halogen atom in the description of the above bivalentgroups include a fluorine atom, a chlorine atom, a bromine atom and aniodine atom.

When Z¹ and Z² each represent a substituted or unsubstituted bivalentaliphatic group, there can be employed any bivalent groups obtained byremoving the hydroxyl groups from the diol of formula (14) in which Yrepresents a bivalent aliphatic group or a bivalent cyclic aliphaticgroup. On the other hand, when Z¹ and Z² each represent a substituted orunsubstituted arylene group, there can be employed any bivalent groupsderived from the substituted or unsubstituted aryl group previouslydefined in the description of R¹, R², Ar⁵ and Ar⁸.

Preferable examples of the diol of formula (14) in which Y represents abivalent aromatic group are as follows:

bis(4-hydroxyphenyl)methane,

bis(2-methyl-4-hydroxyphenyl)methane,

bis(3-methyl-4-hydroxyphenyl)methane,

1,1-bis(4-hydroxyphenyl)ethane

1,2-bis(4-hydroxyphenyl)ethane,

bis(4-hydroxyphenyl)phenylmethane,

bis(4-hydroxyphenyl)diphenylmethane,

1,1-bis(4-hydroxyphenyl)-1-phenylethane,

1,3-bis(4-hydroxyphenyl)-1,1-dimethylpropane,

2,2-bis(4-hydroxyphenyl)propane,

2-(4-hydroxyphenyl)-2-(3-hydroxyphenyl)propane,

1,1-bis(4-hydroxyphenyl)-2-methylpropane,

2,2-bis(4-hydroxyphenyl)butane,

1,1-bis(4-hydroxyphenyl)-3-methylbutane,

2,2-bis(4-hydroxyphenyl)pentane,

2,2-bis(4-hydroxyphenyl)-4-methylpentane,

2,2-bis(4-hydroxyphenyl)hexane,

4,4-bis(4-hydroxyphenyl)heptane,

2,2-bis(4-hydroxyphenyl)nonane,

bis(3,5-dimethyl-4-hydroxyphenyl)methane,

2,2-bis(3-methyl-4-hydroxyphenyl)propane,

2,2-bis(3-isopropyl-4-hydroxyphenyl)propane,

2,2-bis(3-sec-butyl-4-hydroxyphenyl)propane,

2,2-bis(3-tert-butyl-4-hydroxyphenyl)propane,

2,2-bis(3-cyclohexyl-4-hydroxyphenyl)propane,

2,2-bis(3-allyl-4-hydroxyphenyl)propane,

2,2-bis(3-phenyl-4-hydroxyphenyl)propane,

2,2-bis(3,5-dimethyl-4-hydroxyphenyl)propane,

2,2-bis(3-chloro-4-hydroxypheny)propane,

2,2-bis(3,5-dichloro-4-hydroxyphenyl)propane

2,2-bis(3-bromo-4-hydroxyphenyl)propane,

2,2-bis(3,5-dibromo-4-hydroxyphenyl)propane,

2,2-bis(4-hydroxyphenyl)hexafluoropropane,

1,1-bis(4-hydroxyphenyl)cyclopentane,

1,1-bis(4-hydroxyphenyl)cyclohexane,

1,1-bis(3-methyl-4-hydroxyphenyl)cyclohexane,

1,1-bis(3,5-dimethyl-4-hydroxyphenyl)cyclohexane,

1,1-bis(3,5-dichloro-4-hydroxyphenyl)cyclohexane,

1,1-bis(4-hydroxyphenyl)-3,3,5-trimethylcyclohexane,

1,1-bis(4-hydroxyphenyl)cycloheptane,

2,2-bis(4-hydroxyphenyl)norbornane,

2,2-bis(4-hydroxyphenyl)adamantane,

4,4'-dihydroxydiphenyl ether,

4,4'-dihydroxy-3,3'-dimethyldiphenyl ether,

ethylene glycol bis(4-hydroxyphenyl)ether,

4,4'-dihydroxydiphenylsulfide,

3,3'-dimethyl-4,4'-dihydroxydiphenylsulfide,

3,3',5,5'-tetramethyl-4,4'-dihydroxydiphenylsulfide,

4,4'-dihydroxydiphenylsulfoxide,

3,3'-dimethyl-4,4'-dihydroxydiphenylsulfoxide,

4,4'-dihydroxydiphenylsulfone,

3,3'-dimethyl-4,4'-dihydroxydiphenylsulfone,

3,3'-diphenyl-4,4'-dihydroxydiphenylsulfone,

3,3'-dichloro-4,4'-dihydroxydiphenylsulfone,

bis(4-hydroxyphenyl)ketone,

bis(3-methyl-4-hydroxyphenyl)ketone,

3,3,3',3'-tetramethyl-6,6'-dihydroxyspiro(bis)-indane,

3,3',4,4'-tetrahydro-4,4,4',4'-tetramethyl-2,2'-spirobi(2H-1-benzopyrane-7,7'-diol,

trans-2,3-bis(4-hydroxyphenyl)-2-butene,

9,9-bis(4-hydroxyphenyl)fluorene,

9,9-bis(4-hydroxyphenyl)xanthene,

1,6-bis(4-hydroxyphenyl)-1,6-hexanedione,

α,α,α',α'-tetramethyl-α,α'-bis(4-hydroxyphenyl)-p-xylene

α,α,α',α'-tetramethyl-α,α'-bis(4-hydroxyphenyl)-m-xylene

2,6-dihydroxydibenzo-p-dioxine,

2,6-dihydroxythianthrene,

2,7-dihydroxyphenoxathine,

9,10-dimethyl-2,7-dihydroxyphenazine,

3,6-dihydroxydibenzofuran,

3,6-dihydroxydibenzothiophene,

4,4'-dihydroxybiphenyl,

1,4-dihydroxynaphthalene,

2,7-dihydroxypyrene,

hydroquinone,

resorcin,

ethylene glycol-bis(4-hydroxybenzoate),

diethylene glycol-bis(4-hydroxybenzoate),

triethylene glycol-bis(4-hydroxybenzoate),

1,3-bis(4-hydroxyphenyl)-tetramethyldisiloxane,

and

phenol-modified silicone oil.

Further, an aromatic diol having an ester linkage produced by thereaction between 2 moles of a diol and one mole of isophthaloyl chlorideor terephthaloyl chloride is also usable.

In the polycarbonate copolymer resin comprising the structural unit offormula (1) and the structural unit of formula (2), the molar ratio of amoiety composed of the structural unit of formula (1) with respect tothe total amount of the polycarbonate resin may be freely determined,but preferably 5 mol % or more, more preferably 20 mol % or more becausethe total amount of the structural unit of formula (1) has an effect onthe charge transporting properties of the obtained polycarbonate resin.

In the photoconductors according to the present invention, at least oneof the previously mentioned aromatic polycarbonate resins is containedin the photoconductive layers 2, 2a, 2b, 2c, 2d, and 2e. The aromaticpolycarbonate resin can be employed in different ways, for example, asshown in FIGS. 1 through 6.

In the photoconductor as shown in FIG. 1, a photo-conductive layer 2 isformed on an electroconductive support 1, which photoconductive layer 2comprises an aromatic polycarbonate resin of the present invention and asensitizing dye, with the addition thereto of a binder agent (binderresin) when necessary. In this photoconductor, the aromaticpolycarbonate resin works as a photoconductive material, through whichcharge carriers necessary for the light decay of the photoconductor aregenerated and transported. However, the aromatic polycarbonate resinitself scarcely absorbs light in the visible light range, and therefore,it is necessary to add a sensitizing dye which absorbs light in thevisible light range in order to form latent electrostatic images by useof visible light.

Referring to FIG. 2, there is shown an enlarged cross-sectional view ofanother embodiment of an electrophotographic photoconductor according tothe present invention. In this photoconductor, there is formed aphotoconductive layer 2a on an electroconductive support 1. Thephotoconductive layer 2a comprises a charge transport medium 4comprising (i) an aromatic polycarbonate resin of the present invention,optionally in combination with a binder agent, and (ii) a chargegeneration material 3 dispersed in the charge transport medium 4. Inthis embodiment, the aromatic polycarbonate resin (or a mixture of thearomatic polycarbonate resin and the binder agent) constitutes thecharge transport medium 4. The charge generation material 3, which is,for example, an inorganic or organic pigment, generates charge carriers.The charge transport medium 4 accepts the charge carriers generated bythe charge generation material 3 and transports those charge carriers.

In this electrophotographic photoconductor, it is basically necessarythat the light-absorption wavelength regions of the charge generationmaterial 3 and the aromatic polycarbonate resin not overlap in thevisible light range. This is because, in order that the chargegeneration material 3 produce charge carriers efficiently, it isnecessary that light pass through the charge transport medium 4 andreach the surface of the charge generation material 3. Since thearomatic polycarbonate resin comprising the structural unit of formula(1) do not substantially absorb light in the visible range of 600 nm ormore, it can work effectively as a charge transport material when usedtogether with the charge generation material 3 which absorbs the lightin the visible region to the near infrared region and generates chargecarriers. The charge transport medium 4 may further comprise alow-molecular weight charge transport material.

Referring to FIG. 3, there is shown an enlarged cross-sectional view ofa further embodiment of an electrophotographic photoconductor accordingto the present invention. In the figure, there is formed on anelectroconductive support 1 a two-layered photoconductive layer 2bcomprising a charge generation layer 5 containing the charge generationmaterial 3, and a charge transport layer 4 comprising an aromaticpolycarbonate resin with the charge transporting properties according tothe present invention.

In this photoconductor, light which has passed through the chargetransport layer 4 reaches the charge generation layer 5, and chargecarriers are generated within the charge generation layer 5. The chargecarriers which are necessary for the light decay for latentelectrostatic image formation are generated by the charge generationmaterial 3, and accepted and transported by the charge transport layer4. The generation and transportation of the charge carriers areperformed by the same mechanism as that in the photoconductor shown inFIG. 2.

In this case, the charge transport layer 4 comprises the aromaticpolycarbonate resin, optionally in combination with a binder agent.Furthermore, in order to increase the efficiency of generating thecharge carriers, the charge generation layer 5 may further comprise thearomatic polycarbonate resin of the present invention. In addition, thephotoconductive layer 2b including the charge generation layer 5 and thecharge transport layer 4 may further comprise a low-molecular weightcharge transport material for the same reason as mentioned above. Thiscan be applied to the embodiments of FIGS. 4 to 6 to be described later.

As shown in the electrophotographic photoconductor of FIG. 4, aprotective layer 6 may be overlaid on the charge transport layer 4. Theprotective layer 6 may comprise the aromatic polycarbonate resin of thepresent invention, optionally in combination with a binder agent. As amatter of course, it is effective that the protective layer 6 beprovided on a charge transport layer in which a low-molecular weightcharge transport material is dispersed. The protective layer 6 may beprovided on the photoconductive layer 2a of the photoconductor as shownin FIG. 2.

Referring to FIG. 5, there is shown still another embodiment of anelectrophotographic photoconductor according to the present invention.In this figure, the overlaying order of the charge generation layer 5and the charge transport layer 4 comprising the aromatic polycarbonateresin is reversed in view of the electrophotographic photoconductor asshown in FIG. 3. The mechanism of the generation and transportation ofcharge carriers is substantially the same as that of the photoconductorshown in FIG. 3.

In the above photoconductor of FIG. 5, a protective layer 6 may beformed on the charge generation layer 5 as shown in FIG. 6 in light ofthe mechanical strength of the photoconductor.

When the electrophotographic photoconductor according to the presentinvention as shown in FIG. 1 is fabricated, at least one aromaticpolycarbonate resin of the present invention is dissolved in a solvent,with the addition thereto of a binder agent when necessary. To the thusprepared solution, a sensitizing dye is added, so that a photoconductivelayer coating liquid is prepared. The thus prepared photoconductivelayer coating liquid is coated on an electroconductive support 1 anddried, so that a photoconductive layer 2 is formed on theelectroconductive support 1.

It is preferable that the thickness of the photo-conductive layer 2 bein the range of 3 to 50 μm, more preferably in the range of 5 to 40 μm.It is preferable that the amount of the aromatic polycarbonate resin ofthe present invention be in the range of 30 to 100 wt. % of the totalweight of the photoconductive layer 2.

It is preferable that the amount of the sensitizing dye for use in thephotoconductive layer 2 be in the range of 0.1 to 5 wt. %, morepreferably in the range of 0.5 to 3 wt. % of the total weight of thephotoconductive layer 2.

Specific examples of the sensitizing dye for use in the presentinvention are triarylmethane dyes such as Brilliant Green, Victoria BlueB, Methyl Violet, Crystal Violet and Acid Violet 6B; xanthene dyes suchas Rhodamine B, Rhodamine 6G, Rhodamine G Extra, Eosin S, Erythrosin,Rose Bengale and Fluoresceine; thiazine dyes such as Methylene Blue; andcyanine dyes such as cyanin.

The electrophotographic photoconductor shown in FIG. 2 can be obtainedby the following method;

The finely-divided particles of the charge generation material 3 aredispersed in a solution in which at least one aromatic polycarbonateresin of the present invention, or a mixture of the aromaticpolycarbonate resin and the binder agent is dissolved, so that a coatingliquid for the photoconductive layer 2a is prepared. The coating liquidthus prepared is coated on the electroconductive support 1 and thendried, whereby the photoconductive layer 2a is provided on theelectroconductive support 1.

It is proper that the thickness of the photo-conductive layer 2a be inthe range of 3 to 50 μm, more preferably in the range of 5 to 40 μm. Itis preferable that the amount of the aromatic polycarbonate resin foruse in the photoconductive layer 2a be in the range of 40 to less than100 wt. % of the total weight of the photoconductive layer 2a.

It is preferable that the amount of the charge generation material 3 foruse in the photoconductive layer 2a be in the range of 0.1 to 50 wt. %,more preferably in the range of 1 to 20 wt. % of the total weight of thephotoconductive layer 2a.

Specific examples of the charge generation material 3 for use in thepresent invention are as follows: inorganic materials such as selenium,selenium-tellurium, cadmium sulfide, cadmium sulfide-selenium andα-silicon; and organic pigments such as an azo pigment, for example,C.I. Pigment Blue 25 (C.I. 21180), C.I. Pigment Red 41 (C.I. 21200),C.I. Acid Red 52 (C.I. 45100), C.I. Basic Red 3 (C.I. 45210), an azopigment having a carbazole skeleton (Japanese Laid-Open PatentApplication 53-95033), an azo pigment having a distyryl benzene skeleton(Japanese Laid-Open Patent Application 53-133445), an azo pigment havinga triphenylamine skeleton (Japanese Laid-Open Patent Application53-132347), an azo pigment having a dibenzothiophene skeleton (JapaneseLaid-Open Patent Application 54-21728), an azo pigment having anoxadiazole skeleton (Japanese Laid-Open Patent Application 54-12742), anazo pigment having a fluorenone skeleton (Japanese Laid-Open PatentApplication 54-22834), an azo pigment having a bisstilbene skeleton(Japanese Laid-open Patent Application 54-17733), an azo pigment havinga distyryl oxadiazole skeleton (Japanese Laid-Open Patent Application54-2129), and an azo pigment having a distyryl carbazole skeleton(Japanese Laid-Open Patent Application 54-14967); a phthalocyaninepigment such as C.I. Pigment Blue 16 (C.I. 74100); an indigo pigmentsuch as C.I. Vat Brown 5 (C.I. 73410) and C.I. Vat Dye (C.I. 73030); anda perylene pigment such as Algol Scarlet B and Indanthrene Scarlet R(made by Bayer Co., Ltd.). These charge generation materials may be usedalone or in combination.

The electrophotographic photoconductor shown in FIG. 3 can be fabricatedby the following method;

To provide the charge generation layer 5 on the electroconductivesupport 1, the charge generation material is vacuum-deposited on theelectroconductive support 1. Alternatively, the finely-divided particlesof the charge generation material 3 are dispersed in an appropriatesolvent, together with the binder agent when necessary, so that acoating liquid for the charge generation layer 5 is prepared. The thusprepared coating liquid is coated on the electroconductive support 1 anddried, whereby the charge generation layer 5 is formed on theelectroconductive support 1. The charge generation layer 5 may besubjected to surface treatment by buffing and adjustment of thethickness thereof if required. On the thus formed charge generationlayer 5, a coating liquid in which at least one aromatic polycarbonateresin of the present invention, optionally in combination with a binderagent is dissolved is coated and dried, so that the charge transportlayer 4 is formed on the charge generation layer 5. In the chargegeneration layer 5, the same charge generation materials as employed inthe above-mentioned photoconductive layer 2a can be used.

The thickness of the charge generation layer 5 is 5 μm or less,preferably 2 μm or less. It is preferable that the thickness of thecharge transport layer 4 be in the range of 3 to 50 μm, more preferablyin the range of 5 to 40 μm.

When the charge generation layer 5 is provided on the electroconductivesupport 1 by coating the dispersion in which finely-divided particles ofthe charge generation material 3 are dispersed in an appropriatesolvent, it is preferable that the amount of finely-divided particles ofthe charge generation material 3 for use in the charge generation layer5 be in the range of 10 to 100 wt. %, more preferably in the range ofabout 50 to 100 wt. % of the total weight of the charge generation layer5. It is preferable that the amount of the aromatic polycarbonate resinof the present invention for use in the charge transport layer 4 be inthe range of 40 to 100 wt. % of the total weight of the charge transportlayer 4.

The photoconductive layer 2b of the photoconductor shown in FIG. 3 maycomprise a low-molecular-weight charge transport material as previouslymentioned.

Examples of the low-molecular-weight charge transport material for usein the present invention are as follows: oxazole derivatives, oxadiazolederivatives (Japanese Laid-Open Patent Applications 52-139065 and52-139066), imidazole derivatives, triphenylamine derivatives (JapaneseLaid-Open Patent Application 3-285960), benzidine derivatives (JapanesePatent Publication 58-32372), α-phenylstilbene derivatives (JapaneseLaid-Open Patent Application 57-73075), hydrazone derivatives (JapaneseLaid-Open Patent Applications 55-154955, 55-156954, 55-52063, and56-81850), triphenylmethane derivatives (Japanese Patent Publication51-10983), anthracene derivatives (Japanese Laid-Open Patent Application51-94829), styryl derivatives (Japanese Laid-Open Patent Applications56-29245 and 58-198043), carbazole derivatives (Japanese Laid-OpenPatent Application 58-58552), and pyrene derivatives (Japanese Laid-OpenPatent Application 2-94812).

To prepare the photoconductor shown in FIG. 4, a coating liquid for theprotective layer 6 is prepared by dissolving the aromatic polycarbonateresin of the present invention, optionally in combination with thebinder agent, in a solvent, and the thus obtained coating liquid iscoated on the charge transport layer 4 of the photoconductor shown inFIG. 3, and dried.

It is preferable that the thickness of the protective layer 6 be in therange of 0.15 to 10 μm. It is preferable that the amount of the aromaticpolycarbonate resin of the present invention for use in the protectivelayer 6 be in the range of 40 to 100 wt. % of the total weight of theprotective layer 6.

The electrophotographic photoconductor shown in FIG. 5 can be fabricatedby the following method:

The aromatic polycarbonate resin of the present invention, optionally incombination with the binder agent, is dissolved in a solvent to preparea coating liquid for the charge transport layer 4. The thus preparedcoating liquid is coated on the electro-conductive support 1 and dried,whereby the charge transport layer 4 is provided on theelectroconductive support 1. On the thus formed charge transport layer4, a coating liquid prepared by dispersing the finely-divided particlesof the charge generation material 3 in a solvent in which the binderagent may be dissolved when necessary, is coated by spray coating anddried, so that the charge generation layer 5 is provided on the chargetransport layer 4. The amount ratios of the components contained in thecharge generation layer 5 and charge transport layer 4 are the same asthose previously described in FIG. 3.

The electrophotographic photoconductor shown in FIG. 6 can be fabricatedby overlaying a protective layer 6 on the charge generation layer 5 ofthe photoconductor shown in FIG. 5.

To obtain any of the aforementioned photoconductors of the presentinvention, a metallic plate or foil made of aluminum, a plastic film onwhich a metal such as aluminum is deposited, and a sheet of paper whichhas been treated so as to be electro-conductive can be employed as theelectroconductive support 1.

Specific examples of the binder agent used in the preparation of thephotoconductor according to the present invention are condensationresins such as polyamide, polyurethane, polyester, epoxy resin,polyketone and polycarbonate; and vinyl polymers such aspolyvinylketone, polystyrene, poly-N-vinylcarbazole and polyacrylamide.All the resins having electrically insulating properties and adhesionproperties can be employed.

Some plasticizers may be added to the above-mentioned binder agents,when necessary. Examples of the plasticizer for use in the presentinvention are halogenated paraffin, dimethylnaphthalene and dibutylphthalate. Further, a variety of additives such as an antioxidant, alight stabilizer, a thermal stabilizer and a lubricant may also becontained in the binder agents when necessary.

Furthermore, in the electrophotographic photo-conductor according to thepresent invention, an intermediate layer such as an adhesive layer or abarrier layer may be interposed between the electroconductive supportand the photoconductive layer when necessary.

Examples of the material for use in the intermediate layer arepolyamide, nitrocellulose, aluminum oxide, and titanium oxide. It ispreferable that the thickness of the intermediate layer be 1 μm or less.

When copying is performed by use of the photo-conductor according to thepresent invention, the surface of the photoconductor is uniformlycharged to a predetermined polarity in the dark. The uniformly chargedphotoconductor is exposed to a light image so that a latentelectrostatic image is formed on the surface of the photoconductor. Thethus formed latent electrostatic image is developed to a visible imageby a developer, and the developed image can be transferred to a sheet ofpaper when necessary.

The photosensitivity and the durability of the electrophotographicphotoconductor according to the present invention are remarkablyimproved.

Other features of this invention will become apparent in the course ofthe following description of exemplary embodiments, which are given forillustration of the invention and are not intended to be limitingthereof.

Preparation Example 1-1

[Preparation of Aldehyde Compound No. 13 shown in TABLE 3]

In a stream of nitrogen, 77.28 g (504.0 mmol) of phosphorus oxychloridewas added dropwise to 100 ml of N,N-dimethylformamide (DMF) over aperiod of 20 minutes at a temperature of 3 to 6° C. on an ice bath,whereby a Vilsmeier reagent was produced.

To this Vilsmeier reagent, a solution prepared by dissolving 54.67 g(105.0 mmol) of a diamine compound represented by the following formula(26) in 300 ml of DMF was added dropwise at 6° C. over a period of 30minutes. ##STR1445##

The temperature of the reaction mixture was returned to room temperatureover a period of 30 minutes with stirring, and the reaction mixture washeated to 86° C. and stirred for 3 hours. Then, the reaction mixture wasallowed to stand at room temperature, and poured into 2000 ml ofice-cold water. With the addition of a 20% aqueous solution of sodiumhydroxide, the reaction mixture was made basic, and stirred at roomtemperature for 2 hours. The resultant yellow precipitate was extractedwith ethyl acetate, and the resultant organic layer was washed withwater and dried over anhydrous magnesium sulfate. The ethyl acetate wasdistilled away from the reaction mixture under reduced pressure, therebyobtaining a yellow-black oily material.

This material was then chromatographed on silica gel and eluted with amixed solvent of toluene and ethyl acetate (at a ratio by volume of20:1), so that an aldehyde compound No. 13 shown in TABLE 3 was obtainedas yellow crystals in a yield of 47.16 g (77.9%).

The melting point of this compound was 155.5 to 157.5° C.

The results of the elemental analysis of the thus obtained product wereas follows:

    ______________________________________                                                 % C        % H    % N                                                ______________________________________                                        Found      79.14        4.89   4.86                                             Calculated 79.31 4.96 4.74                                                  ______________________________________                                    

The calculation is based on the formula for C₃₈ H₂₈ N₂ O₂ S.

FIG. 7 is an infrared spectrum of the aldehyde compound No. 13 by use ofa KBr tablet.

Preparation Examples 1-2 and 1-3.

The procedure for preparation of the aldehyde compound No. 13 inPreparation Example 1-1 was repeated except that the diamine compound offormula (26) used in Preparation Example 1-1 was replaced by eachdiamine compound shown in the following TABLE 4, so that aldehydecompounds No. 1 and No. 7 (shown in TABLE 3) for use in the presentinvention were respectively obtained in Preparation Examples 1-2 and1-3.

The melting point, and the results of the elemental analysis of eachaldehyde compound are shown in TABLE 4.

FIG. 8 and FIG. 9 show infrared spectra of the aldehyde compounds No. 1and No. 7, respectively.

                                      TABLE 4                                     __________________________________________________________________________         Aldehyde                                                                   Prepara- Compound Elemental Analysis                                        tion No.                                           % C % H % N                  Example (See Diamine Compound Melting Found Found Found                       No. TABLE 3) (Raw Material) Point (° C.) (Calcd.)  (Calcd.)                                                                     (Calcd.)           __________________________________________________________________________      1-1 13                                                                                                                                 4  155.5-157.5                                                                79.14 (79.31)                                                                 4.89 (4.96)                                                                   4.86 (4.74)                                                                     - 1-2 1                                                                     5  160.5-161.5                                                                84.23 (83.39)                                                                 5.59 (5.63)                                                                   4.74 (4.89)                                                                     - 1-3 7                                                                     6  149.5-152.5                                                                81.25 (81.41)                                                                 5.00 (5.03)                                                                   4.91 (5.00)        __________________________________________________________________________

Preparation Example 2-1

(Preparation of Aminostilbene Compound 1 shown in TABLE 2)

14.32 g (25.0 mmol) of the aldehyde compound No. 1 (shown in TABLE 3)represented by the following formula, synthesized in Preparation Example1-2, and 15.49 g (60.0 mmol) of diethyl 4-methoxybenzyl phosphonate wereplaced in 100 ml of DMF.

[Aldehyde compound No. 1] ##STR1449##

With stirring the above prepared mixture, 6.73 g (60.0 mmol) ofpotassium t-butoxide was added thereto over a period of 10 minutes, sothat the reaction was carried out at room temperature for 3 hours.

This reaction mixture was poured into 400 ml of ice-cold water, andneutralized by the addition thereto of acetic acid. The resultantprecipitate was separated from the reaction mixture by filtration, andsuccessively washed with water and methanol, and then dried.

Thereafter, the obtained material was chromatographed on silica gel andeluted with a mixed solvent of toluene and cyclohexane (at a ratio byvolume of 3:2), so that an aminostilbene compound No. 1 shown in TABLE 2was obtained as light yellow crystals in a yield of 17.99 g (92.2%).

The melting point of this compound was 215.5 to 218.5° C.

The results of the elemental analysis of the thus obtained product wereas follows:

    ______________________________________                                                 % C        % H    % N                                                ______________________________________                                        Found      86.42        6.44   3.28                                             Calculated 86.12 6.19 3.59                                                  ______________________________________                                    

The calculation is based on the formula for C₅₆ H₄₈ N₂ O₂.

FIG. 10 is an infrared spectrum of the aminostilbene compound No. 1 byuse of a KBr tablet.

Preparation Examples 2-2 to 2-4

The procedure for preparation of the aminostilbene compound No. 1 inPreparation Example 2-1 was repeated except that the aldehyde compoundNo. 1 and diethyl 4-methoxybenzyl phosphonate used in PreparationExample 2-1 were replaced by the respective raw materials shown in thefollowing TABLE 5, so that aminostilbene compounds No. 12, No. 13 andNo. 14 (shown in TABLE 2) for use in the present invention wererespectively obtained in Preparation Examples 2-2, 2-3, and 2-4.

The melting point, and the results of the elemental analysis of eachaminostilbene compound are shown in TABLE 5.

FIG. 11, FIG. 12 and FIG. 13 show infrared spectra of the aminostilbenecompounds No. 12, No. 13 and No. 14, respectively.

    TABLE 5       -  Amino-        stilbene        Com-       Prepa- pound  Elemental Anaylsis       ration No. Raw Materials Melting % C % H % N       Example (See Aldehyde Compound Phosphorus-containing Point Found Found     F ound       No. TABLE 2) (See TABLE 3) Compound (° C.) (Calcd.) (Calcd.)     (Calcd.)       2-2 12      ##STR1450##     1      ##STR1451##     2  272 (Endo- thermic peak by DTA) 84.25 (84.34) 5.66 (5.78) 3.58 (3.64)        (No. 7)     2-3 13      ##STR1452##     1      ##STR1453##     3  197.5- 201.5 84.95 (84.34) 5.87 (5.78) 3.39 (3.00)        (No. 7)     2-4 14      ##STR1454##     4      ##STR1455##     2  250 82.59 (82.62) 5.57 (5.65) 3.60 (3.57)        (No. 13)

Preparation Example 3-1

(Preparation of Diol Compound 1 shown in TABLE 1)

15.62 g (20.0 mmol) of the aminostilbene compound No. 1 represented bythe following formula, synthesized in Preparation Example 2-1, and 10 g(107 mmol) of 90% sodium thioethylate were added to 100 ml ofN,N-dimethylforamide dried using molecular sieves. The thus preparedmixture was stirred at 130 to 135° C. in a stream of nitrogen for 3hours.

[Aminostilbene Compound No. 1] ##STR1456##

After the reaction mixture was cooled to 60° C., the mixture was pouredinto 300 ml of ice-cold water, and made acid with concentratedhydrochloric acid, and then stirred at room temperature for one hour.The precipitating crystals were separated from the reaction mixture byfiltration, and successively washed with water and methanol, and thendried.

Thereafter, the obtained material was chromatographed on silica gel andeluted with a mixed solvent of toluene and ethyl acetate (at a ratio byvolume of 10:1), so that a diol compound (hydroxystilbene compound ) No.1 shown in TABLE 1 was obtained as yellow crystals in a yield of 12.04 g(79.9%).

The melting point of this compound was 213.5 to 218.0° C.

The results of the elemental analysis of the thus obtained product wereas follows:

    ______________________________________                                                 % C        % H    % N                                                ______________________________________                                        Found      86.12        5.83   3.59                                             Calculated 86.14 5.89 3.72                                                  ______________________________________                                    

The calculation is based on the formula for C₅₄ H₄₄ N₂ O₂.

FIG. 14 is an infrared spectrum of the diol compound No. 1 by use of aKBr tablet.

Preparation Examples 3-2 and 3-3

The procedure for preparation of the diol compound No. 1 in PreparationExample 3-1 was repeated except that the aminostilbene compound No. 1used in Preparation Example 3-1 was replaced by each aminostilbenecompound shown in the following TABLE 6, so that diol compounds No. 12and No. 14 (shown in TABLE 1) for use in the present invention wererespectively obtained in Preparation Examples 3-2 and 3-3.

The melting point, and the results of the elemental analysis of eachdiol compound are shown in TABLE 6.

FIG. 15 and FIG. 16 show infrared spectra of the diol compounds No. 12and No. 14, respectively.

                                      TABLE 6                                     __________________________________________________________________________                  Aminostilbene                                                                             Elemental Analysis                                         Diol   Compound No.                                                                          Melting                                                                           % C  % H % N                                          Preparation Compound No. (Raw Material) Point Found  Found  Found                                               Example No. (See TABLE 1) (See TABLE                                         2) (° C.) (Calcd.) (Calcd.)                                            (Calcd.)                                   __________________________________________________________________________    3-1    1      1       213.5-                                                                            86.12                                                                              5.63                                                                              3.59                                            218.0 (86.14) (5.89) (3.72)                                                3-2 12 12 >250 84.34  5.38  3.57                                                  (84.30) (5.44) (3.78)                                                     3-3 14 14 235.0 82.47  5.29  3.71                                                 (82.51) (5.33) (3.70)                                                   __________________________________________________________________________

EXAMPLE 1-1

(Synthesis of Aromatic Polycarbonate Resin No. 1)

In a stream of nitrogen a mixture of 2.26 g (3.0 mmol) of the diolcompound No. 1 (shown in TABLE 1) represented by the following formula,synthesized in Preparation Example 3-1 and 0.91 g (9.0 mmol) oftriethylamine was dissolved in 15 ml of dry tetrahydrofuran at roomtemperature.

[Diol compound No. 1] ##STR1457##

To the above prepared mixture, a solution prepared by dissolving 1.10 g(3.0 mmol) of tetraethylene glycol bis(chloroformate) in 3 ml of drytetrahydrofuran was added dropwise over a period of 30 minutes. Then,the reaction mixture was stirred at room temperature for 3 hours. Withthe addition of 0.21 g of a 4% tetrahydrofuran solution of phenol, thereaction mixture was further stirred for one hour.

The resultant precipitating triethylamine hydrochloride was removed fromthe reaction mixture by filtration, and the residual filtrate (that is,tetrahydrofuran solution) was added dropwise to methanol. The thusprecipitating product was separated by filtration, and dried by theapplication of heat thereto under reduced pressure.

Further, the thus obtained crude product was purified by repeating theprocess of dissolving the product in tetrahydrofuran and precipitatingit in methanol twice, and the obtained resin was dried by theapplication of heat thereto under reduced pressure, so that an aromaticpolycarbonate resin No. 1 according to the present invention wasobtained as an alternating copolymer having a repeat unit shown in TABLE8 in a yield of 2.36 g (75.2%).

The glass transition temperature (Tg) of the aromatic polycarbonateresin No. 1 was 82.3° C.

The polystyrene-reduced number-average molecular weight andweight-average molecular weight, which were measured by the gelpermeation chromatography, were respectively 21,700 and 41,500.

The results of the elemental analysis of the thus obtained compound areas follows:

    ______________________________________                                                 % C        % H    % N                                                ______________________________________                                        Found      78.44        6.52   2.66                                             Calculated 78.51 6.43 2.68                                                  ______________________________________                                    

The calculation is based on the formula for C₆₈.36 H₆₆.72 N₂ O₈.09,

FIG. 17 shows an infrared spectrum of the aromatic polycarbonate resinNo. 1, taken by use of a cast film.

EXAMPLE 1-2 and 1-3 (Synthesis of Aromatic Polycarbonate Resins Nos. 2and 3)

The procedure for preparation of the aromatic polycarbonate resin No. 1in Example 1-1 was repeated except that tetraethylene glycolbis(chloroformate) used in Example 1-1 was replaced by eachbis(chloroformate) compound shown in TABLE 7A.

Thus, aromatic polycarbonate resins No. 2 and No. 3 according to thepresent invention were obtained, each having the repeat unit shown inTABLE 8.

The glass transition temperature (Tg), the polystyrene-reducednumber-average molecular weight (Mn), the polystyrene-reducedweight-average molecular weight.(Mw), and the results of the elementalanalysis of each of the obtained aromatic polycarbonate resins No. 2 andNo. 3 are shown in TABLE 8.

FIGS. 18 and 19 respectively show infrared spectra of the aromaticpolycarbonate resins No. 2 and No. 3 obtained in Examples 1-2 and 1-3,taken by use of a cast film.

EXAMPLE 1-4

1.355 g (1.80 mmol) of the diol compound No. 1 synthesized inPreparation Example 3-1, 1.065 g (4.67 mmol) of bisphenol A, and 0.020 gof t-butylphenol were placed in a reaction vessel. In a stream of argon,the above prepared mixture was stirred with the addition thereto of 50ml of ion exchange water in which 0.071 g of hydrosulfite and 1.035 g ofsodium hydroxide were dissolved.

To the above reaction mixture, 35 ml of dichloromethane in which 1.152 gof triphosgene was dissolved was added dropwise at 3° C., and thereafterthe temperature of the reaction mixture was returned to room temperatureover a period of 15 minutes. Then, 1.5 ml of 10% sodium hydroxide andtwo drops of triethylamrine were successively added to the reactionmixture to carry out the reaction for 2 hours.

With the addition of 0.010 g of t-butylphenol, the reaction mixture wasfurther stirred for 2 hours. The thus obtained reaction mixture wasprecipitated in methanol, so that an aromatic polycarbonate resin No. 4according to the present invention was obtained as a random copolymerhaving structural units shown in TABLE 8 was obtained in a yield of 2.49g (96.1%).

The glass transition temperature (Tg) of the aromatic polycarbonateresin No. 4 was 171.2° C.

The polystyrene-reduced number-average molecular weight andweight-average molecular weight, which were measured by the gelpermeation chromatography, were respectively 28,400 and 127,400.

The results of the elemental analysis of the thus obtained compound areas follows:

    ______________________________________                                                 % C        % H    % N                                                ______________________________________                                        Found      80.44        5.37   2.13                                             Calculated 80.56 5.49 1.96                                                  ______________________________________                                    

The calculation is based on the formula for C₂₆.94 H₂₁.78 N₀.56 O₃.

FIG. 20 shows an infrared spectrum of the aromatic polycarbonate resinNo. 4, taken by use of a cast film.

EXAMPLE 1-5 and 1-8 (Synthesis of Aromatic Polycarbonate Resins Nos. 5to 8)

The procedure for preparation of the aromatic polycarbonate resin No. 4in Example 1-4 was repeated except that the diol compound No. 1 andbisphenol A used in Example 1-4 were replaced by the respective diolcompounds shown in TABLE 7B.

Thus, aromatic polycarbonate resins No. 5 to No. 8 according to thepresent invention were obtained, each having the structural units shownin TABLE 8.

The glass transition temperature (Tg), the polystyrene-reducednumber-average molecular weight (Mn), the polystyrene-reducedweight-average molecular weight (Mw), and the results of the elementalanalysis of each of the obtained aromatic polycarbonate resins No. 5 toNo. 8 are shown in TABLE 8.

FIGS. 21, 22, 23 and 24 respectively show infrared spectra of thearomatic polycarbonate resins Nos. 5, 6, 7 and 8 obtained in Examples1-5, 1-6, 1-7 and 1-8, taken by use of a cast film.

    TABLE 7A       -   Poly-       Ex- Raw Materials carbo-       ample Diol with charge transporting properties Bis(chloroformate nate     Re-       No. (See TABLE 1) compound) sin No.       1-1      ##STR1458##     5      ##STR1459##     6  1       (Diol No. 1)     1-2      ##STR1460##     5      ##STR1461##     7  2       (Diol No. 1)       1-3      ##STR1462##     5      ##STR1463##     8  3       (Diol No. 1)

    TABLE 7B       -   Poly-       Ex- Raw Materials carbo-       ample Diol with charge transporting properties Bis(chloroformate nate     Re-       No. (See TABLE 1) compound) sin No.       1-4      ##STR1464##     5      ##STR1465##     9  4       (Diol No. 1)     1-5      ##STR1466##     5      ##STR1467##     0  5       (Diol No. 1)       1-6      ##STR1468##     1      ##STR1469##     9  6       (Diol No. 12)       1-7      ##STR1470##     1      ##STR1471##     2  7       (Diol No. 12)       1-8      ##STR1472##     3      ##STR1473##     2  8       (Diol No. 14)

    TABLE 8       - Poly-       carbo-  Elemental Analysis       Exam- nate  Molecular % C % H % N       ple Resin  Weight Found Found Found Tg       No. No. Structure of Polycarbonate Resin Mn Mw (Calcd.) (Calcd.)     (Calcd.) (°      C.)       1-1 1      ##STR1474##     4  21700 41500 78.44 (78.51) 6.52 (6.43) 2.66 (2.68) 82.3     1-2 2      ##STR1475##     5  23400 60800 80.56 (80.67) 5.96 (5.90) 3.06 (3.04) 136.3     1-3 3      ##STR1476##     6  5700 10800 82.76 (82.53) 5.49 (5.46) 2.78 (2.71) 146.1     1-4 4      ##STR1477##     7  28400 127400 80.44 (80.56) 5.37 (5.49) 2.13 (1.96) 171.2     1-5 5      ##STR1478##     8  46600 142500 81.44 (81.48) 5.74 (5.77) 2.24 (1.95) 173.9     1-6 6      ##STR1479##     9  46600 139000 79.49 (79.61) 5.13 (5.25) 2.01 (1.98) 183.7     1-7 7      ##STR1480##     0  45000 143700 80.01 (80.06) 5.58 (5.65) 1.97 (1.98) 160.9     1-8 8      ##STR1481##     1  44000 143600 79.02 (79.14) 5.52 (5.60) 1.89 (1.94) 164.8

EXAMPLE 2-1

[Fabrication of Photoconductor No. 1]

(Formation of intermediate layer)

A commercially available polyamide resin (Trademark "CM-8000", made byToray Industries, Inc.) was dissolved in a mixed solvent of methanol andbutanol, so that a coating liquid for an intermediate layer wasprepared.

The thus prepared coating liquid was coated on an aluminum plate by adoctor blade, and dried at room temperature, so that an intermediatelayer with a thickness of 0.3 μm was provided on the aluminum plate.(Formation of charge generation layer)

A coating liquid for a charge generation layer was prepared bypulverizing and dispersing a bisazo compound of the following formula,serving as a charge generation material, in a mixed solvent ofcyclohexanone and 2-butanone in a ball mill. The thus obtained coatingliquid was coated on the above prepared intermediate layer by a doctorblade, and dried at room temperature. Thus, a charge generation layerwith a thickness of 0.5 μm was formed on the intermediate layer.

<Bisazo compound> ##STR1482## (Formation of charge transport layer)

The aromatic polycarbonate resin No. 1 shown in TABLE 8, prepared inExample 1-1, which served as a charge transport material, was dissolvedin dichloromethane. The thus obtained coating liquid was coated on theabove prepared charge generation layer by a doctor blade, and dried atroom temperature and then at 120° C. for 20 minutes, so that a chargetransport layer with a thickness of 20 μm was provided on the chargegeneration layer.

Thus, an electrophotographic photoconductor No. 1 according to thepresent invention was fabricated.

EXAMPLES 2-2 to 2-8

The procedure for fabrication of the layered electrophotographicphotoconductor No. 1 in Example 2-1 was repeated except that thearomatic polycarbonate resin No. 1 for use in the charge transport layercoating liquid in Example 2-1 was replaced by each of the aromaticpolycarbonate resins shown in TABLE 9.

Thus, electrophotographic photoconductors No. 2 to No. 8 according tothe present invention were fabricated.

Each of the electrophotographic photoconductors No. 1 through No. 8according to the present invention obtained in Examples 2-1 to 2-8 wascharged negatively in the dark under application of -6 kV of coronacharge for 20 seconds, using a commercially available electrostaticcopying sheet testing apparatus ("Paper Analyzer Model SP-428" made byKawaguchi Electro Works Co., Ltd.). The surface potential Vm (V) wasmeasured.

Then, each electrophotographic photoconductor was allowed to stand inthe dark for 20 seconds without applying any charge thereto, and thesurface potential Vo (V) of the photoconductor was measured.

Each photoconductor was then illuminated by a tungsten lamp in such amanner that the illuminance on the illuminated surface of thephotoconductor was 4.5 lux, and the exposure E_(1/2) (lux.sec) requiredto reduce the surface potential Vo (V) to 1/2 the surface potential Vo(V) was measured.

The results are shown in TABLE 9.

                  TABLE 9                                                         ______________________________________                                                  Aromatic                                                              Example Polycarbonate -Vm -Vo E.sub.1/2                                       No. Resin No. (V) (V) (lux · sec)                                  ______________________________________                                        2-1       No. 1      1323     1030 1.06                                         2-2 No. 2 1470 1205 1.17                                                      2-3 No. 3  637  507 0.79                                                      2-4 No. 4 1591 1382 1.11                                                      2-5 No. 5 1582 1363 1.07                                                      2-6 No. 6 1490 1295 1.06                                                      2-7 No. 7 1590 1386 1.08                                                      2-8 No. 8 1575 1378 1.10                                                    ______________________________________                                    

Furthermore, each of the above obtained electrophotographicphotoconductors No. 1 to No. 8 was set in a commercially availableelectrophotographic copying machine, and the photoconductor was chargedand exposed to light images via the original images to form latentelectrostatic images thereon. Then, the latent electrostatic imagesformed on the photoconductor were developed into visible toner images bya dry developer, and the visible toner images were transferred to asheet of plain paper and fixed thereon. As a result, clear toner imageswere obtained on the paper. When a wet developer was employed for theimage formation, clear images were formed on the paper similarly.

As previously explained, the aromatic polycarbonate resin according tothe present invention has the charge transporting properties and highmechanical strength, so that the photosensitivity and durability of thephotoconductor are sufficiently high when the aromatic polycarbonateresin is used in the photoconductive layer.

Japanese Patent Application No. 09-153846 filed Jun. 11, 1997, JapanesePatent Application No. 09-153988 filed Jun. 11, 1997, Japanese PatentApplication No. 09-326324 filed Nov. 27, 1997, Japanese PatentApplication No. 10-160845 filed Jun. 9, 1998, Japanese PatentApplication No. 10- 160853 filed Jun. 9, 1998, Japanese PatentApplication No. 10-162207 filed Jun. 10, 1998, and Japanese PatentApplication No. 10-162228 filed Jun. 10, 1998 are hereby incorporated byreference.

What is claimed is:
 1. An electrophotographic photoconductor comprisingan electroconductive support, and a photoconductive layer formed thereoncomprising as an effective component an aromatic polycarbonate resincomprising a structural unit of formula (1): ##STR1483## wherein R¹ andR², which may be the same or different, are each a hydrogen atom, analkyl group which may have a substituent, or an aryl group which mayhave a substituent; Ar¹, Ar², Ar³, Ar⁴, Ar⁶ and Ar⁷, which may be thesame or different, are each an arylene group which may have asubstituent; Ar⁵ and Ar⁸, which may be the same or different, are eachan aryl group which may have a substituent; X is --O--, --S--, --SO--,--SO₂ --, --CO--, a straight-chain, branched or cyclic alkylene grouphaving 1 to 12 carbon atoms, or an arylene group which may have asubstituent; and s is an integer of 0 or
 1. 2. An electrophotographicphotoconductor comprising an electroconductive support, and aphotoconductive layer formed thereon comprising as an effectivecomponent an aromatic polycarbonate resin comprising a structural unitof formula (1) and a structural unit of formula (2), with a compositionratio of said structural unit of formula (1) to said structural unit offormula (2) satisfying a relationship of 0<k/(k+j)≦1, wherein k is amoiety ratio of said structural unit of formula (1) and j is a moietyratio of said structural unit of formula (2) in said aromaticpolycarbonate resin: ##STR1484## wherein R¹ and R², which may be thesame or different, are each a hydrogen atom, an alkyl group which mayhave a substituent, or an aryl group which may have a substituent; Ar¹,Ar², Ar³, Ar⁴, Ar⁶ and Ar⁷, which may be the same or different, are eachan arylene group which may have a substituent; Ar⁵ and Ar⁶, which may bethe same or different, are each an aryl group which may have asubstituent; X is --O--, --S--, --SO--, --SO₂ --, --CO--, astraight-chain, branched or cyclic alkylene group having 1 to 12 carbonatoms, or an arylene group which may have a substituent; s is an integerof 0 or 1; and Y is a bivalent aliphatic group, a bivalent cyclicaliphatic group, a bivalent aromatic group, a bivalent group obtained bybonding the above-mentioned bivalent groups, or ##STR1485## in which R³,R⁴, R⁵ and R⁶ are each independently an alkyl group which may have asubstituent, an aryl group which may have a substituent, or a halogenatom; a and b are each independently an integer of 0 to 4; c and d areeach independently an integer of 0 to 3; and m is an integer of 0 or 1,provided that when m=1, Z is a straight-chain alkylene group having 2 to12 carbon atoms, --O--, --S--, --SO--, --SO₂ --, --CO--, ##STR1486## inwhich Z¹ and Z² are each a bivalent aliphatic group which may have asubstituent or an arylene group which may have a substituent; and R⁷,R⁸, R⁹, R¹⁰, R¹¹, R¹² and R¹³ are each independently a hydrogen atom, ahalogen atom, an alkyl group having 1 to 5 carbon atoms which may have asubstituent, an alkoxyl group having 1 to 5 carbon atoms which may havea substituent, or an aryl group which may have a substituent, and R⁷ andR⁸ may form a carbocyclic ring or heterocyclic ring having 6 to 12carbon atoms in combination, or may form a carbocyclic ring orheterocyclic ring in combination with R³ and R⁴ ; p and q are each aninteger of 0 or 1, provided that when p and q represent 1, R¹⁴ and R¹⁵are each an alkylene group having 1 to 4 carbon atoms; R¹⁶ and R¹⁷ areeach independently an alkyl group having 1 to 5 carbon atoms which mayhave a substituent, or an aryl group which may have a substituent; e isan integer of 0 to 4; f is an integer of 0 to 20; and g is an integer of0 to
 2000. 3. The electrophotographic photoconductor as claimed in claim1, wherein said structural unit of formula (1) is represented by formula(4): ##STR1487## wherein R¹, R², Ar⁵, Ar⁸, X and s are respectively thesame as defined in formula (1).
 4. The electrophotographicphotoconductor as claimed in claim 3, wherein said structural unit offormula (4) is represented by formula (6): ##STR1488## wherein R₁, R²,Ar⁵, Ar⁸, X and s are respectively the same as defined in formula (4).5. The electrophotographic photoconductor as claimed in claim 4, whereinsaid structural unit of formula (6) is represented by formula (8):##STR1489## wherein R¹, R², X and s are respectively the same as definedin formula (6); and R¹⁸ and R¹⁹, which may be the same or different, areeach a hydrogen atom, an alkyl group which may have a substituent, or anaryl group which may have a substituent.
 6. The electrophotographicphotoconductor as claimed in claim 2, wherein said structural unit offormula (1) is represented by formula (4): ##STR1490## wherein R¹, R²,Ar⁵, Ar⁸, X and s are respectively the same as defined in formula (1).7. The electrophotographic photoconductor as claimed in claim 6, whereinsaid structural unit of formula (4) is represented by formula (6)##STR1491## wherein R¹, R², Ar⁵, Ar⁸, X and s are respectively the sameas defined in formula (4).
 8. The electrophotographic photoconductor asclaimed in claim 7, wherein said structural unit of formula (6) isrepresented by formula (8) ##STR1492## wherein R¹, R², X and s arerespectively the same as defined in formula (6); and R¹⁸ and R¹⁹, whichmay be the same or different, are each a hydrogen atom, an alkyl groupwhich may have a substituent, or an aryl group which may have asubstituent.
 9. An electrophotographic photoconductor comprising anelectroconductive support, and a photoconductive layer formed thereoncomprising as an effective component an aromatic polycarbonate resincomprising a repeat unit of formula (3): ##STR1493## wherein R¹ and R²,which may be the same or different, are each a hydrogen atom, an alkylgroup which may have a substituent, or an aryl group which may have asubstituent; Ar¹, Ar², Ar³, Ar⁴, Ar⁶ and Ar⁷, which may be the same ordifferent, are each an arylene group which may have a substituent; Ar⁵and Ar⁸, which may be the same or different, are each an aryl groupwhich may have a substituent; X is --O--, --S--, --SO--, --SO₂ --,--CO--, a straight-chain, branched or cyclic alkylene group having 1 to12 carbon atoms, or an arylene group which may have a substituent; s isan integer of 0 or 1; n is an integer of 2 to 5000; and Y is a bivalentaliphatic group, a bivalent cyclic aliphatic group, a bivalent aromaticgroup, a bivalent group obtained by bonding the above-mentioned bivalentgroups, or ##STR1494## in which R³, R⁴, R⁵ and R⁶ are each independentlyan alkyl group which may have a substituent, an aryl group which mayhave a substituent, or a halogen atom; a and b are each independently aninteger of 0 to 4; c and d are each independently an integer of 0 to 3;and m is an integer of 0 or 1, provided that when m=1, Z is astraight-chain alkylene group having 2 to 12 carbon atoms, --O--, --S--,--SO₂ --, --CO--, ##STR1495## in which Z¹ and Z² are each a bivalentaliphatic group which may have a substituent or an arylene group whichmay have a substituent; and R⁷, R⁸, R⁹, R¹⁰, R¹¹, R¹² and R¹³ are eachindependently a hydrogen atom, a halogen atom, an alkyl group having 1to 5 carbon atoms which may have a substituent, an alkoxyl group having1 to 5 carbon atoms which may have a substituent, or an aryl group whichmay have a substituent, and R⁷ and R⁸ may form a carbocyclic ring orheterocyclic ring having 6 to 12 carbon atoms in combination, or mayform a carbocyclic ring or heterocyclic ring in combination with R³ andR⁴ ; p and q are each an integer of 0 or 1, provided that when p and qrepresent 1, R¹⁴ and R¹⁵ are each an alkylene group having 1 to 4 carbonatoms; R¹⁶ and R¹⁷ are each independently an alkyl group having 1 to 5carbon atoms which may have a substituent, or an aryl group which mayhave a substituent; e is an integer of 0 to 4; f is an integer of 0 to20; and g is an integer of 0 to
 2000. 10. The electrophotographicphotoconductor as claimed in claim 9, wherein said repeat unit offormula (3) is represented by formula (5): ##STR1496## wherein R¹, R²,Ar⁵, Ar⁸, s, X, Y and n are respectively the same as defined in formula(3).
 11. The electrophotographic photoconductor as claimed in claim 10,wherein said repeat unit of formula (5) is represented by formula (7):##STR1497## wherein R¹, R², Ar⁵, Ar⁸, s, X, Y and n are respectively thesame as defined in formula (5).
 12. The electrophotographicphotoconductor as claimed in claim 11, wherein said repeat unit offormula (7) is represented by formula (9): ##STR1498## wherein R¹, R²,s, X, Y and n are respectively the same as defined in formula (7); andR¹⁸ and R¹³, which may be the same or different, are each a hydrogenatom, an alkyl group which may have a substituent, or an aryl groupwhich may have a substituent.